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rs121909666

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909666(A;A)
Make rs121909666(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position30233692
GeneFSHB
is asnp
is mentioned by
dbSNPrs121909666
ebirs121909666
HLIrs121909666
Exacrs121909666
Varsomers121909666
Maprs121909666
PheGenIrs121909666
hapmaprs121909666
1000 genomesrs121909666
hgdprs121909666
ensemblrs121909666
gopubmedrs121909666
geneviewrs121909666
scholarrs121909666
googlers121909666
pharmgkbrs121909666
gwascentralrs121909666
openSNPrs121909666
23andMers121909666
23andMe allrs121909666
SNP Nexus

SNPshotrs121909666
SNPdbers121909666
MSV3drs121909666
GWAS Ctlgrs121909666
Max Magnitude0
OMIM136530
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121909666(A;A)
Alt rs121909666(A;A)
Reference rs121909666(C;C)
Significance Pathogenic
Disease Follicle-stimulating hormone deficiency
Variation info
Gene FSHB
CLNDBN Follicle-stimulating hormone deficiency, isolated
Reversed 0
HGVS NC_000011.9:g.30255239C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017629.28,