chr11:13492716:C>A Detail (hg38) (PTH)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr11:13,514,263-13,514,263 View the variant detail on this assembly version. |
hg38 | chr11:13,492,716-13,492,716 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_000315.3:c.87-50G>T | |
NM_001316352.1:c.87-50G>T | ||
Ensemble | ENST00000282091.6:c.87-50G>T |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:[No Data.] | |
NCBN:[No Data.] | |
NCBN(Hondo):[No Data.] | |
NCBN(Ryukyu):[No Data.] | |
East asia | ExAC:<0.001 |
Prediction
ClinVar
Clinical Significance | |
Review star | [No Data.] |
Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
<0.001 | aortic valve stenosis | Finally, rs1544410 polymorphism within the VDR gene, E2 and E4 alleles within th... | BeFree | 24903972 | Detail |
0.003 | aortic valve stenosis | Finally, rs1544410 polymorphism within the VDR gene, E2 and E4 alleles within th... | BeFree | 24903972 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
Finally, rs1544410 polymorphism within the VDR gene, E2 and E4 alleles within the apoE gene, rs6254 ... | DisGeNET | Detail |
Finally, rs1544410 polymorphism within the VDR gene, E2 and E4 alleles within the apoE gene, rs6254 ... | DisGeNET | Detail |
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- Genome
- hg38
- Position
- chr11:13,492,716-13,492,716
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- A
- East Asian Chromosome Counts (ExAC)
- 8570
- East Asian Allele Counts (ExAC)
- 0
- East Asian Heterozygous Counts (ExAC)
- 0
- East Asian Homozygous Counts (ExAC)
- 0
- East Asian Allele Frequency (ExAC)
- 0.0
- Chromosome Counts in All Race (ExAC)
- 120366
- Allele Counts in All Race (ExAC)
- 1
- Heterozygous Counts in All Race (ExAC)
- 1
- Homozygous Counts in All Race (ExAC)
- 0
- Allele Frequency in All Race (ExAC)
- 8.307993951780402E-6
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