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rs137852664

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852664(C;T)
Make rs137852664(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position101770378
GeneFGF8
is asnp
is mentioned by
dbSNPrs137852664
ebirs137852664
HLIrs137852664
Exacrs137852664
Varsomers137852664
Maprs137852664
PheGenIrs137852664
hapmaprs137852664
1000 genomesrs137852664
hgdprs137852664
ensemblrs137852664
gopubmedrs137852664
geneviewrs137852664
scholarrs137852664
googlers137852664
pharmgkbrs137852664
gwascentralrs137852664
openSNPrs137852664
23andMers137852664
23andMe allrs137852664
SNP Nexus

SNPshotrs137852664
SNPdbers137852664
MSV3drs137852664
GWAS Ctlgrs137852664
Max Magnitude0
OMIM600483
Desc
Variant0006
Relatedalso
ClinVar
Risk rs137852664(T;T)
Alt rs137852664(T;T)
Reference rs137852664(C;C)
Significance Unknown
Disease Kallmann syndrome 6
Variation info
Gene FGF8
CLNDBN Kallmann syndrome 6
Reversed 1
HGVS NC_000010.10:g.103530135G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009697.2,