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rs121909659

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121909659(C;C)
Make rs121909659(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position48989022
GeneFSHR
is asnp
is mentioned by
dbSNPrs121909659
ebirs121909659
HLIrs121909659
Exacrs121909659
Varsomers121909659
Maprs121909659
PheGenIrs121909659
hapmaprs121909659
1000 genomesrs121909659
hgdprs121909659
ensemblrs121909659
gopubmedrs121909659
geneviewrs121909659
scholarrs121909659
googlers121909659
pharmgkbrs121909659
gwascentralrs121909659
openSNPrs121909659
23andMers121909659
23andMe allrs121909659
SNP Nexus

SNPshotrs121909659
SNPdbers121909659
MSV3drs121909659
GWAS Ctlgrs121909659
Max Magnitude0
OMIM136435
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121909659(C;C)
Alt rs121909659(C;C)
Reference rs121909659(T;T)
Significance Pathogenic
Disease Ovarian dysgenesis 1
Variation info
Gene FSHR
CLNDBN Ovarian dysgenesis 1
Reversed 1
HGVS NC_000002.11:g.49216161A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000017631.24,