rs104894136
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs104894136(C;T) |
Make rs104894136(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 10 |
Position | 102834074 |
Gene | CYP17A1, CYP17A1-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs104894136 |
dbSNP (classic) | rs104894136 |
ClinGen | rs104894136 |
ebi | rs104894136 |
HLI | rs104894136 |
Exac | rs104894136 |
Gnomad | rs104894136 |
Varsome | rs104894136 |
LitVar | rs104894136 |
Map | rs104894136 |
PheGenI | rs104894136 |
Biobank | rs104894136 |
1000 genomes | rs104894136 |
hgdp | rs104894136 |
ensembl | rs104894136 |
geneview | rs104894136 |
scholar | rs104894136 |
rs104894136 | |
pharmgkb | rs104894136 |
gwascentral | rs104894136 |
openSNP | rs104894136 |
23andMe | rs104894136 |
SNPshot | rs104894136 |
SNPdbe | rs104894136 |
MSV3d | rs104894136 |
GWAS Ctlg | rs104894136 |
Max Magnitude | 0 |
c.715C>T (p.Arg239Ter)
23andMe name: i5001494
ClinVar | |
---|---|
Risk | rs104894136(T;T) |
Alt | rs104894136(T;T) |
Reference | Rs104894136(C;C) |
Significance | Other |
Disease | Combined partial 17-alpha-hydroxylase/17 Breast cancer |
Variation | info |
Gene | CYP17A1 |
CLNDBN | Combined partial 17-alpha-hydroxylase/17,20-lyase deficiency Breast cancer, susceptibility to |
Reversed | 1 |
HGVS | NC_000010.10:g.104593831G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000001854.2, RCV000001855.2, |