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rs137852659

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852659(A;A)
Make rs137852659(A;C)
ReferenceGRCh38 38.1/141
Chromosome10
Position101775769
GeneFGF8
is asnp
is mentioned by
dbSNPrs137852659
ebirs137852659
HLIrs137852659
Exacrs137852659
Varsomers137852659
Maprs137852659
PheGenIrs137852659
hapmaprs137852659
1000 genomesrs137852659
hgdprs137852659
ensemblrs137852659
gopubmedrs137852659
geneviewrs137852659
scholarrs137852659
googlers137852659
pharmgkbrs137852659
gwascentralrs137852659
openSNPrs137852659
23andMers137852659
23andMe allrs137852659
SNP Nexus

SNPshotrs137852659
SNPdbers137852659
MSV3drs137852659
GWAS Ctlgrs137852659
Max Magnitude0
OMIM600483
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137852659(A;A)
Alt rs137852659(A;A)
Reference rs137852659(C;C)
Significance Pathogenic
Disease Kallmann syndrome 6
Variation info
Gene FGF8
CLNDBN Kallmann syndrome 6
Reversed 1
HGVS NC_000010.10:g.103535526G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000030886.2,