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rs137852661

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852661(C;C)
Make rs137852661(C;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position101775168
GeneFGF8
is asnp
is mentioned by
dbSNPrs137852661
ebirs137852661
HLIrs137852661
Exacrs137852661
Varsomers137852661
Maprs137852661
PheGenIrs137852661
hapmaprs137852661
1000 genomesrs137852661
hgdprs137852661
ensemblrs137852661
gopubmedrs137852661
geneviewrs137852661
scholarrs137852661
googlers137852661
pharmgkbrs137852661
gwascentralrs137852661
openSNPrs137852661
23andMers137852661
23andMe allrs137852661
SNP Nexus

SNPshotrs137852661
SNPdbers137852661
MSV3drs137852661
GWAS Ctlgrs137852661
Max Magnitude0
OMIM600483
Desc
Variant0003
Relatedalso
ClinVar
Risk rs137852661(C;C)
Alt rs137852661(C;C)
Reference rs137852661(T;T)
Significance Pathogenic
Disease Kallmann syndrome 6
Variation info
Gene FGF8
CLNDBN Kallmann syndrome 6
Reversed 1
HGVS NC_000010.10:g.103534925A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000030887.2,