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

rs387906427

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906427(G;T)
Make rs387906427(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position8570498
GeneKAL1
is asnp
is mentioned by
dbSNPrs387906427
ebirs387906427
HLIrs387906427
Exacrs387906427
Varsomers387906427
Maprs387906427
PheGenIrs387906427
hapmaprs387906427
1000 genomesrs387906427
hgdprs387906427
ensemblrs387906427
gopubmedrs387906427
geneviewrs387906427
scholarrs387906427
googlers387906427
pharmgkbrs387906427
gwascentralrs387906427
openSNPrs387906427
23andMers387906427
23andMe allrs387906427
SNP Nexus

SNPshotrs387906427
SNPdbers387906427
MSV3drs387906427
GWAS Ctlgrs387906427
Max Magnitude0
ClinVar
Risk rs387906427(T;T)
Alt rs387906427(T;T)
Reference rs387906427(G;G)
Significance Pathogenic
Disease Kallmann syndrome 1
Variation info
Gene KAL1 ANOS1
CLNDBN Kallmann syndrome 1
Reversed 1
HGVS NC_000023.10:g.8538539C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010698.2,