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rs137852663

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852663(C;G)
Make rs137852663(G;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position101771528
GeneFGF8
is asnp
is mentioned by
dbSNPrs137852663
ebirs137852663
HLIrs137852663
Exacrs137852663
Varsomers137852663
Maprs137852663
PheGenIrs137852663
hapmaprs137852663
1000 genomesrs137852663
hgdprs137852663
ensemblrs137852663
gopubmedrs137852663
geneviewrs137852663
scholarrs137852663
googlers137852663
pharmgkbrs137852663
gwascentralrs137852663
openSNPrs137852663
23andMers137852663
23andMe allrs137852663
SNP Nexus

SNPshotrs137852663
SNPdbers137852663
MSV3drs137852663
GWAS Ctlgrs137852663
Max Magnitude0
OMIM600483
Desc
Variant0005
Relatedalso
ClinVar
Risk rs137852663(G;G)
Alt rs137852663(G;G)
Reference rs137852663(C;C)
Significance Pathogenic
Disease Kallmann syndrome 6
Variation info
Gene FGF8
CLNDBN Kallmann syndrome 6
Reversed 1
HGVS NC_000010.10:g.103531285G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000009695.2,