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rs121909658

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909658(C;T)
Make rs121909658(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position48983125
GeneFSHR
is asnp
is mentioned by
dbSNPrs121909658
ebirs121909658
HLIrs121909658
Exacrs121909658
Varsomers121909658
Maprs121909658
PheGenIrs121909658
hapmaprs121909658
1000 genomesrs121909658
hgdprs121909658
ensemblrs121909658
gopubmedrs121909658
geneviewrs121909658
scholarrs121909658
googlers121909658
pharmgkbrs121909658
gwascentralrs121909658
openSNPrs121909658
23andMers121909658
23andMe allrs121909658
SNP Nexus

SNPshotrs121909658
SNPdbers121909658
MSV3drs121909658
GWAS Ctlgrs121909658
Max Magnitude0
OMIM136435
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909658(T;T)
Alt rs121909658(T;T)
Reference rs121909658(C;C)
Significance Pathogenic
Disease Ovarian dysgenesis 1
Variation info
Gene FSHR
CLNDBN Ovarian dysgenesis 1
Reversed 1
HGVS NC_000002.11:g.49210264G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017630.29,