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rs764841861

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs764841861(C;T)
Make rs764841861(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position100204096
GeneGATS, STAG3
is asnp
is mentioned by
dbSNPrs764841861
dbSNP (classic)rs764841861
ClinGenrs764841861
ebirs764841861
HLIrs764841861
Exacrs764841861
Gnomadrs764841861
Varsomers764841861
LitVarrs764841861
Maprs764841861
PheGenIrs764841861
Biobankrs764841861
1000 genomesrs764841861
hgdprs764841861
ensemblrs764841861
geneviewrs764841861
scholarrs764841861
googlers764841861
pharmgkbrs764841861
gwascentralrs764841861
openSNPrs764841861
23andMers764841861
SNPshotrs764841861
SNPdbers764841861
MSV3drs764841861
GWAS Ctlgrs764841861
Max Magnitude0
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,