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rs121909660

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909660(C;T)
Make rs121909660(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position48963104
GeneFSHR
is asnp
is mentioned by
dbSNPrs121909660
ebirs121909660
HLIrs121909660
Exacrs121909660
Varsomers121909660
Maprs121909660
PheGenIrs121909660
hapmaprs121909660
1000 genomesrs121909660
hgdprs121909660
ensemblrs121909660
gopubmedrs121909660
geneviewrs121909660
scholarrs121909660
googlers121909660
pharmgkbrs121909660
gwascentralrs121909660
openSNPrs121909660
23andMers121909660
23andMe allrs121909660
SNP Nexus

SNPshotrs121909660
SNPdbers121909660
MSV3drs121909660
GWAS Ctlgrs121909660
Max Magnitude0
OMIM136435
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121909660(T;T)
Alt rs121909660(T;T)
Reference rs121909660(C;C)
Significance Pathogenic
Disease Ovarian dysgenesis 1
Variation info
Gene FSHR
CLNDBN Ovarian dysgenesis 1
Reversed 1
HGVS NC_000002.11:g.49190243G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017632.29,