chr19:6718376:G>C Detail (hg38) (C3)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr19:6,718,387-6,718,387 View the variant detail on this assembly version. |
hg38 | chr19:6,718,376-6,718,376 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_000064.3:c.304C>G | NP_000055.2:p.Arg102Gly |
Ensemble | ENST00000245907.11:c.304C>G | ENST00000245907.11:p.Arg102Gly |
ENST00000695693.1:c.304C>G | ENST00000695693.1:p.Arg102Gly |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:0.001 |
ToMMo:[No Data.] | |
NCBN:[No Data.] | |
NCBN(Hondo):[No Data.] | |
NCBN(Ryukyu):[No Data.] | |
East asia | ExAC:<0.001 |
Prediction
ClinVar
Clinical Significance |
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Review star | ![]() |
Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
---|---|---|---|---|---|
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2013-04-01 | no assertion criteria provided | MACULAR DEGENERATION, AGE-RELATED, 9, SUSCEPTIBILITY TO |
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Detail |
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2013-04-01 | no assertion criteria provided | C3S/C3F POLYMORPHISM |
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Detail |
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2017-04-27 | criteria provided, single submitter | age related macular degeneration 9 |
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Detail |
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2024-02-01 | criteria provided, multiple submitters, no conflicts | not provided |
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Detail |
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2022-09-27 | criteria provided, single submitter |
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Detail | |
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2015-01-23 | criteria provided, single submitter | Inborn genetic diseases |
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Detail |
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.319 | age related macular degeneration | Seventeen single nucleotide polymorphisms (SNPs) in known AMD risk-associated ge... | BeFree | 23582991 | Detail |
0.480 | age related macular degeneration | Seventeen single nucleotide polymorphisms (SNPs) in known AMD risk-associated ge... | BeFree | 23582991 | Detail |
0.021 | age related macular degeneration | Seventeen single nucleotide polymorphisms (SNPs) in known AMD risk-associated ge... | BeFree | 23582991 | Detail |
0.005 | age related macular degeneration | Seventeen single nucleotide polymorphisms (SNPs) in known AMD risk-associated ge... | BeFree | 23582991 | Detail |
0.311 | age related macular degeneration | Seven new loci associated with age-related macular degeneration. | GWASCAT | 23455636 | Detail |
0.311 | age related macular degeneration | Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-rela... | GWASCAT | 21665990 | Detail |
0.311 | age related macular degeneration | Genome-wide association identifies SKIV2L and MYRIP as protective factors for ag... | GWASCAT | 20861866 | Detail |
0.311 | age related macular degeneration | [implicate different biologic pathways than previously reported and provide new ... | GAD | 20385826 | Detail |
0.311 | age related macular degeneration | Genetic variants near TIMP3 and high-density lipoprotein-associated loci influen... | GWASCAT | 20385819 | Detail |
0.311 | age related macular degeneration | [Genetic variants near TIMP3 and high-density lipoprotein-associated loci influe... | GAD | 20385819 | Detail |
0.311 | age related macular degeneration | Genome-wide association study of advanced age-related macular degeneration ident... | GWASCAT | 20385826 | Detail |
0.311 | age related macular degeneration | We investigated the association between the LOC387715 A69S and complement compon... | BeFree | 19048105 | Detail |
0.311 | age related macular degeneration | Heritability and genome-wide association study to assess genetic differences bet... | GWASCAT | 22705344 | Detail |
0.311 | age related macular degeneration | [Complement component 3: an assessment of association with AMD and analysis of g... | GAD | 20157618 | Detail |
0.010 | Geographic Atrophy | Analyzing the currently largest dataset on GA lesion growth (N = 388), our findi... | BeFree | 25962167 | Detail |
0.082 | obesity | Moreover, in exploratory analyses, we identified a number of possible interactio... | BeFree | 24287500 | Detail |
0.480 | age related macular degeneration | Moreover, in exploratory analyses, we identified a number of possible interactio... | BeFree | 24287500 | Detail |
0.001 | obesity | Moreover, in exploratory analyses, we identified a number of possible interactio... | BeFree | 24287500 | Detail |
0.311 | age related macular degeneration | Moreover, in exploratory analyses, we identified a number of possible interactio... | BeFree | 24287500 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_000064.4(C3):c.304C>G (p.Arg102Gly) AND MACULAR DEGENERATION, AGE-RELATED, 9, SUSCEPTIBILITY TO | ClinVar | Detail |
NM_000064.4(C3):c.304C>G (p.Arg102Gly) AND C3S/C3F POLYMORPHISM | ClinVar | Detail |
NM_000064.4(C3):c.304C>G (p.Arg102Gly) AND Age related macular degeneration 9 | ClinVar | Detail |
NM_000064.4(C3):c.304C>G (p.Arg102Gly) AND not provided | ClinVar | Detail |
NM_000064.4(C3):c.304C>G (p.Arg102Gly) AND Focal segmental glomerulosclerosis | ClinVar | Detail |
NM_000064.4(C3):c.304C>G (p.Arg102Gly) AND Inborn genetic diseases | ClinVar | Detail |
Seventeen single nucleotide polymorphisms (SNPs) in known AMD risk-associated genes including CFH (r... | DisGeNET | Detail |
Seventeen single nucleotide polymorphisms (SNPs) in known AMD risk-associated genes including CFH (r... | DisGeNET | Detail |
Seventeen single nucleotide polymorphisms (SNPs) in known AMD risk-associated genes including CFH (r... | DisGeNET | Detail |
Seventeen single nucleotide polymorphisms (SNPs) in known AMD risk-associated genes including CFH (r... | DisGeNET | Detail |
Seven new loci associated with age-related macular degeneration. | DisGeNET | Detail |
Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degenera... | DisGeNET | Detail |
Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular de... | DisGeNET | Detail |
[implicate different biologic pathways than previously reported and provide new avenues for preventi... | DisGeNET | Detail |
Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to... | DisGeNET | Detail |
[Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility t... | DisGeNET | Detail |
Genome-wide association study of advanced age-related macular degeneration identifies a role of the ... | DisGeNET | Detail |
We investigated the association between the LOC387715 A69S and complement component C3 R102G risk al... | DisGeNET | Detail |
Heritability and genome-wide association study to assess genetic differences between advanced age-re... | DisGeNET | Detail |
[Complement component 3: an assessment of association with AMD and analysis of gene-gene and gene-en... | DisGeNET | Detail |
Analyzing the currently largest dataset on GA lesion growth (N = 388), our findings suggest a signif... | DisGeNET | Detail |
Moreover, in exploratory analyses, we identified a number of possible interactions including between... | DisGeNET | Detail |
Moreover, in exploratory analyses, we identified a number of possible interactions including between... | DisGeNET | Detail |
Moreover, in exploratory analyses, we identified a number of possible interactions including between... | DisGeNET | Detail |
Moreover, in exploratory analyses, we identified a number of possible interactions including between... | DisGeNET | Detail |
Overlapped Transcript Coordinates
Gene | Transcript ID | Exon Number | Chromosome | Start | Stop | Type | Amino Mutation | Transcript Position | Links |
---|
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs2230199 dbSNP
- Genome
- hg38
- Position
- chr19:6,718,376-6,718,376
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- C
- Filtering Status (HGVD)
- PASS
- # of samples (HGVD)
- 1210
- Mean of sample read depth (HGVD)
- 156.33
- Standard deviation of sample read depth (HGVD)
- 71.29
- Number of reference allele (HGVD)
- 2417
- Number of alternative allele (HGVD)
- 3
- Allele Frequency (HGVD)
- 0.0012396694214876034
- Gene Symbol (HGVD)
- C3
- East Asian Chromosome Counts (ExAC)
- 8654
- East Asian Allele Counts (ExAC)
- 4
- East Asian Heterozygous Counts (ExAC)
- 4
- East Asian Homozygous Counts (ExAC)
- 0
- East Asian Allele Frequency (ExAC)
- 4.6221400508435407E-4
- Chromosome Counts in All Race (ExAC)
- 121366
- Allele Counts in All Race (ExAC)
- 18423
- Heterozygous Counts in All Race (ExAC)
- 14919
- Homozygous Counts in All Race (ExAC)
- 1752
- Allele Frequency in All Race (ExAC)
- 0.15179704365308241
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