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rs121909661

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909661(A;A)
Make rs121909661(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position48963566
GeneFSHR
is asnp
is mentioned by
dbSNPrs121909661
ebirs121909661
HLIrs121909661
Exacrs121909661
Varsomers121909661
Maprs121909661
PheGenIrs121909661
hapmaprs121909661
1000 genomesrs121909661
hgdprs121909661
ensemblrs121909661
gopubmedrs121909661
geneviewrs121909661
scholarrs121909661
googlers121909661
pharmgkbrs121909661
gwascentralrs121909661
openSNPrs121909661
23andMers121909661
23andMe allrs121909661
SNP Nexus

SNPshotrs121909661
SNPdbers121909661
MSV3drs121909661
GWAS Ctlgrs121909661
Max Magnitude0
OMIM136435
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121909661(A;A)
Alt rs121909661(A;A)
Reference rs121909661(G;G)
Significance Pathogenic
Disease Ovarian dysgenesis 1
Variation info
Gene FSHR
CLNDBN Ovarian dysgenesis 1
Reversed 1
HGVS NC_000002.11:g.49190705C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017636.31,