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rs137852515

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852515(A;A)
Make rs137852515(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position8536852
GeneKAL1
is asnp
is mentioned by
dbSNPrs137852515
ebirs137852515
HLIrs137852515
Exacrs137852515
Varsomers137852515
Maprs137852515
PheGenIrs137852515
hapmaprs137852515
1000 genomesrs137852515
hgdprs137852515
ensemblrs137852515
gopubmedrs137852515
geneviewrs137852515
scholarrs137852515
googlers137852515
pharmgkbrs137852515
gwascentralrs137852515
openSNPrs137852515
23andMers137852515
23andMe allrs137852515
SNP Nexus

SNPshotrs137852515
SNPdbers137852515
MSV3drs137852515
GWAS Ctlgrs137852515
Merged fromRs28937309
Max Magnitude0
OMIM308700
Desc
Variant0007
Relatedalso
ClinVar
Risk rs137852515(A;A)
Alt rs137852515(A;A)
Reference rs137852515(G;G)
Significance Pathogenic
Disease Kallmann syndrome 1
Variation info
Gene ANOS1
CLNDBN Kallmann syndrome 1
Reversed 1
HGVS NC_000023.10:g.8504893C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010691.6,