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rs398124648

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398124648(G;G)
Make rs398124648(G;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position47161748
GeneCALM2
is asnp
is mentioned by
dbSNPrs398124648
ebirs398124648
HLIrs398124648
Exacrs398124648
Varsomers398124648
Maprs398124648
PheGenIrs398124648
hapmaprs398124648
1000 genomesrs398124648
hgdprs398124648
ensemblrs398124648
gopubmedrs398124648
geneviewrs398124648
scholarrs398124648
googlers398124648
pharmgkbrs398124648
gwascentralrs398124648
openSNPrs398124648
23andMers398124648
23andMe allrs398124648
SNP Nexus

SNPshotrs398124648
SNPdbers398124648
MSV3drs398124648
GWAS Ctlgrs398124648
Max Magnitude0
ClinVar
Risk rs398124648(G;G)
Alt rs398124648(G;G)
Reference rs398124648(T;T)
Significance Pathogenic
Disease Long QT syndrome 1 Long QT syndrome 15
Variation info
Gene CALM2
CLNDBN Long QT syndrome 1 Long QT syndrome 15
Reversed 1
HGVS NC_000002.11:g.47388887A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000143838.1, RCV000162069.2,