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rs121909663

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121909663(A;G)
Make rs121909663(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position48963476
GeneFSHR
is asnp
is mentioned by
dbSNPrs121909663
ebirs121909663
HLIrs121909663
Exacrs121909663
Varsomers121909663
Maprs121909663
PheGenIrs121909663
hapmaprs121909663
1000 genomesrs121909663
hgdprs121909663
ensemblrs121909663
gopubmedrs121909663
geneviewrs121909663
scholarrs121909663
googlers121909663
pharmgkbrs121909663
gwascentralrs121909663
openSNPrs121909663
23andMers121909663
23andMe allrs121909663
SNP Nexus

SNPshotrs121909663
SNPdbers121909663
MSV3drs121909663
GWAS Ctlgrs121909663
Max Magnitude0
OMIM136435
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121909663(G;G)
Alt rs121909663(G;G)
Reference rs121909663(A;A)
Significance Pathogenic
Disease Ovarian hyperstimulation syndrome
Variation info
Gene FSHR
CLNDBN Ovarian hyperstimulation syndrome
Reversed 1
HGVS NC_000002.11:g.49190615T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000017640.28,