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rs137852662

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852662(A;G)
Make rs137852662(G;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position101774771
GeneFGF8
is asnp
is mentioned by
dbSNPrs137852662
ebirs137852662
HLIrs137852662
Exacrs137852662
Varsomers137852662
Maprs137852662
PheGenIrs137852662
hapmaprs137852662
1000 genomesrs137852662
hgdprs137852662
ensemblrs137852662
gopubmedrs137852662
geneviewrs137852662
scholarrs137852662
googlers137852662
pharmgkbrs137852662
gwascentralrs137852662
openSNPrs137852662
23andMers137852662
23andMe allrs137852662
SNP Nexus

SNPshotrs137852662
SNPdbers137852662
MSV3drs137852662
GWAS Ctlgrs137852662
Max Magnitude0
OMIM600483
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137852662(G;G)
Alt rs137852662(G;G)
Reference rs137852662(A;A)
Significance Pathogenic
Disease Kallmann syndrome 6
Variation info
Gene FGF8
CLNDBN Kallmann syndrome 6
Reversed 1
HGVS NC_000010.10:g.103534528T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000030888.4,