Have questions? Visit https://www.reddit.com/r/SNPedia

rs137852660

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852660(C;T)
Make rs137852660(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position101775209
GeneFGF8
is asnp
is mentioned by
dbSNPrs137852660
ebirs137852660
HLIrs137852660
Exacrs137852660
Varsomers137852660
Maprs137852660
PheGenIrs137852660
hapmaprs137852660
1000 genomesrs137852660
hgdprs137852660
ensemblrs137852660
gopubmedrs137852660
geneviewrs137852660
scholarrs137852660
googlers137852660
pharmgkbrs137852660
gwascentralrs137852660
openSNPrs137852660
23andMers137852660
23andMe allrs137852660
SNP Nexus

SNPshotrs137852660
SNPdbers137852660
MSV3drs137852660
GWAS Ctlgrs137852660
GMAF0.0004591
Max Magnitude0
OMIM600483
Desc
Variant0002
Relatedalso
ClinVar
Risk rs137852660(T;T)
Alt rs137852660(T;T)
Reference rs137852660(C;C)
Significance Pathogenic
Disease Kallmann syndrome 6 not specified
Variation info
Gene FGF8
CLNDBN Kallmann syndrome 6 not specified
Reversed 1
HGVS NC_000010.10:g.103534966G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009692.2, RCV000239300.1,