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rs121909662

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909662(A;A)
Make rs121909662(A;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position48963266
GeneFSHR
is asnp
is mentioned by
dbSNPrs121909662
ebirs121909662
HLIrs121909662
Exacrs121909662
Varsomers121909662
Maprs121909662
PheGenIrs121909662
hapmaprs121909662
1000 genomesrs121909662
hgdprs121909662
ensemblrs121909662
gopubmedrs121909662
geneviewrs121909662
scholarrs121909662
googlers121909662
pharmgkbrs121909662
gwascentralrs121909662
openSNPrs121909662
23andMers121909662
23andMe allrs121909662
SNP Nexus

SNPshotrs121909662
SNPdbers121909662
MSV3drs121909662
GWAS Ctlgrs121909662
Max Magnitude0
OMIM136435
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121909662(A;A)
Alt rs121909662(A;A)
Reference rs121909662(C;C)
Significance Pathogenic
Disease Ovarian dysgenesis 1
Variation info
Gene FSHR
CLNDBN Ovarian dysgenesis 1
Reversed 1
HGVS NC_000002.11:g.49190405G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017639.23,