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rs121909664

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121909664(C;C)
Make rs121909664(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position48963187
GeneFSHR
is asnp
is mentioned by
dbSNPrs121909664
ebirs121909664
HLIrs121909664
Exacrs121909664
Varsomers121909664
Maprs121909664
PheGenIrs121909664
hapmaprs121909664
1000 genomesrs121909664
hgdprs121909664
ensemblrs121909664
gopubmedrs121909664
geneviewrs121909664
scholarrs121909664
googlers121909664
pharmgkbrs121909664
gwascentralrs121909664
openSNPrs121909664
23andMers121909664
23andMe allrs121909664
SNP Nexus

SNPshotrs121909664
SNPdbers121909664
MSV3drs121909664
GWAS Ctlgrs121909664
Max Magnitude0
OMIM136435
Desc
Variant0012
Relatedalso
ClinVar
Risk rs121909664(C;C)
Alt rs121909664(C;C)
Reference rs121909664(T;T)
Significance Pathogenic
Disease Ovarian hyperstimulation syndrome
Variation info
Gene FSHR
CLNDBN Ovarian hyperstimulation syndrome
Reversed 1
HGVS NC_000002.11:g.49190326A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000017641.28,