chr1:11862778:A>G Detail (hg19) (MTHFR)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr1:11,862,778-11,862,778 |
hg38 | chr1:11,802,721-11,802,721 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_005957.4:c.236+160T>C | |
Ensemble | ENST00000376583.7:c.359+160T>C | |
ENST00000423400.7:c.356+160T>C |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:0.104 | |
NCBN:[No Data.] | |
NCBN(Hondo):[No Data.] | |
NCBN(Ryukyu):[No Data.] | |
East asia | ExAC:[No Data.] |
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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2018-07-27 | criteria provided, single submitter | not provided |
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Detail |
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
<0.001 | Hypertensive disease | The genetic risk score, calculated as the sum of BP-increasing alleles of FGF5-r... | BeFree | 20852445 | Detail |
0.002 | Hypertensive disease | The genetic risk score, calculated as the sum of BP-increasing alleles of FGF5-r... | BeFree | 20852445 | Detail |
0.127 | Systemic arterial pressure | [Genome-wide association study identifies six new loci influencing pulse pressur... | GAD | 21909110 | Detail |
0.125 | Blood pressure finding | [Genome-wide association study identifies eight loci associated with blood press... | GAD | 19430483 | Detail |
0.127 | Systemic arterial pressure | [Genome-wide association study identifies eight loci associated with blood press... | GAD | 19430483 | Detail |
0.125 | Blood pressure finding | [Genome-wide association study identifies six new loci influencing pulse pressur... | GAD | 21909110 | Detail |
0.127 | Systemic arterial pressure | Genome-wide association study identifies six new loci influencing pulse pressure... | GWASCAT | 21909110 | Detail |
0.125 | Blood pressure finding | Genome-wide association study identifies six new loci influencing pulse pressure... | GWASCAT | 21909110 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_005957.5(MTHFR):c.236+160T>C AND not provided | ClinVar | Detail |
The genetic risk score, calculated as the sum of BP-increasing alleles of FGF5-rs16998073, CYP17A1-r... | DisGeNET | Detail |
The genetic risk score, calculated as the sum of BP-increasing alleles of FGF5-rs16998073, CYP17A1-r... | DisGeNET | Detail |
[Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial ... | DisGeNET | Detail |
[Genome-wide association study identifies eight loci associated with blood pressure.] | DisGeNET | Detail |
[Genome-wide association study identifies eight loci associated with blood pressure.] | DisGeNET | Detail |
[Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial ... | DisGeNET | Detail |
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial p... | DisGeNET | Detail |
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial p... | DisGeNET | Detail |
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs17367504 dbSNP
- Genome
- hg19
- Position
- chr1:11,862,778-11,862,778
- Variant Type
- snv
- Reference Allele
- A
- Alternative Allele
- G
- ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- PASS
- Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- rs17367504
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.1039
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 1742
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
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