rs764841861
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs764841861(C;T) |
Make rs764841861(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 7 |
Position | 100204096 |
Gene | GATS, STAG3 |
is a | snp |
is | mentioned by |
dbSNP | rs764841861 |
dbSNP (classic) | rs764841861 |
ClinGen | rs764841861 |
ebi | rs764841861 |
HLI | rs764841861 |
Exac | rs764841861 |
Gnomad | rs764841861 |
Varsome | rs764841861 |
LitVar | rs764841861 |
Map | rs764841861 |
PheGenI | rs764841861 |
Biobank | rs764841861 |
1000 genomes | rs764841861 |
hgdp | rs764841861 |
ensembl | rs764841861 |
geneview | rs764841861 |
scholar | rs764841861 |
rs764841861 | |
pharmgkb | rs764841861 |
gwascentral | rs764841861 |
openSNP | rs764841861 |
23andMe | rs764841861 |
SNPshot | rs764841861 |
SNPdbe | rs764841861 |
MSV3d | rs764841861 |
GWAS Ctlg | rs764841861 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs764841861(T;T) |
Alt | rs764841861(T;T) |
Reference | Rs764841861(C;C) |
Significance | Probable-Pathogenic |
Disease | Female infertility Premature ovarian failure Abnormality of the ovary |
Variation | info |
Gene | STAG3 GATS |
CLNDBN | Female infertility Premature ovarian failure Abnormality of the ovary |
Reversed | 0 |
HGVS | NC_000007.13:g.99801719C>T |
CLNSRC | |
CLNACC | RCV000415001.1, RCV000415224.1, |