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rs397518425

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397518425(-;-)
Make rs397518425(-;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position8539662
GeneKAL1
is asnp
is mentioned by
dbSNPrs397518425
ebirs397518425
HLIrs397518425
Exacrs397518425
Varsomers397518425
Maprs397518425
PheGenIrs397518425
hapmaprs397518425
1000 genomesrs397518425
hgdprs397518425
ensemblrs397518425
gopubmedrs397518425
geneviewrs397518425
scholarrs397518425
googlers397518425
pharmgkbrs397518425
gwascentralrs397518425
openSNPrs397518425
23andMers397518425
23andMe allrs397518425
SNP Nexus

SNPshotrs397518425
SNPdbers397518425
MSV3drs397518425
GWAS Ctlgrs397518425
Max Magnitude0
ClinVar
Risk rs397518425(;)
Alt rs397518425(;)
Reference rs397518425(T;T)
Significance Pathogenic
Disease Kallmann syndrome 1
Variation info
Gene ANOS1
CLNDBN Kallmann syndrome 1
Reversed 1
HGVS NC_000023.10:g.8507703delA
CLNSRC ClinVar Seth G.S. Medical College and K.E.M. Hospital
CLNACC RCV000074341.2,