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rs121909665

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909665(A;A)
Make rs121909665(A;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position48990629
GeneFSHR
is asnp
is mentioned by
dbSNPrs121909665
ebirs121909665
HLIrs121909665
Exacrs121909665
Varsomers121909665
Maprs121909665
PheGenIrs121909665
hapmaprs121909665
1000 genomesrs121909665
hgdprs121909665
ensemblrs121909665
gopubmedrs121909665
geneviewrs121909665
scholarrs121909665
googlers121909665
pharmgkbrs121909665
gwascentralrs121909665
openSNPrs121909665
23andMers121909665
23andMe allrs121909665
SNP Nexus

SNPshotrs121909665
SNPdbers121909665
MSV3drs121909665
GWAS Ctlgrs121909665
Max Magnitude0
OMIM136435
Desc
Variant0013
Relatedalso
ClinVar
Risk rs121909665(A;A)
Alt rs121909665(A;A)
Reference rs121909665(C;C)
Significance Pathogenic
Disease Ovarian hyperstimulation syndrome
Variation info
Gene FSHR
CLNDBN Ovarian hyperstimulation syndrome
Reversed 1
HGVS NC_000002.11:g.49217768G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017642.24,