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rs28928871

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0
(G;G) 0 common in clinvar
Make rs28928871(A;A)
Make rs28928871(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position48963122
GeneFSHR
is asnp
is mentioned by
dbSNPrs28928871
ebirs28928871
HLIrs28928871
Exacrs28928871
Varsomers28928871
Maprs28928871
PheGenIrs28928871
hapmaprs28928871
1000 genomesrs28928871
hgdprs28928871
ensemblrs28928871
gopubmedrs28928871
geneviewrs28928871
scholarrs28928871
googlers28928871
pharmgkbrs28928871
gwascentralrs28928871
openSNPrs28928871
23andMers28928871
23andMe allrs28928871
SNP Nexus

SNPshotrs28928871
SNPdbers28928871
MSV3drs28928871
GWAS Ctlgrs28928871
Max Magnitude0
OMIM136435
DescOVARIAN HYPERSTIMULATION SYNDROME
Variant0009
Relatedalso
Neighborrs6166
Distance340
Neighborrs28928870
Distance353


ClinVar
Risk rs28928871(A;A)
Alt rs28928871(A;A)
Reference rs28928871(G;G)
Significance Pathogenic
Disease Ovarian hyperstimulation syndrome
Variation info
Gene FSHR
CLNDBN Ovarian hyperstimulation syndrome
Reversed 1
HGVS NC_000002.11:g.49190261C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017638.28,