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

rs137852512

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852512(A;A)
Make rs137852512(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position8587809
GeneKAL1
is asnp
is mentioned by
dbSNPrs137852512
ebirs137852512
HLIrs137852512
Exacrs137852512
Varsomers137852512
Maprs137852512
PheGenIrs137852512
hapmaprs137852512
1000 genomesrs137852512
hgdprs137852512
ensemblrs137852512
gopubmedrs137852512
geneviewrs137852512
scholarrs137852512
googlers137852512
pharmgkbrs137852512
gwascentralrs137852512
openSNPrs137852512
23andMers137852512
23andMe allrs137852512
SNP Nexus

SNPshotrs137852512
SNPdbers137852512
MSV3drs137852512
GWAS Ctlgrs137852512
Max Magnitude0
OMIM308700
Desc
Variant0002
Relatedalso
ClinVar
Risk rs137852512(A;A)
Alt rs137852512(A;A)
Reference rs137852512(G;G)
Significance Pathogenic
Disease Kallmann syndrome 1
Variation info
Gene KAL1 ANOS1
CLNDBN Kallmann syndrome 1
Reversed 1
HGVS NC_000023.10:g.8555850C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010686.6,