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rs398124649

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398124649(A;C)
Make rs398124649(C;C)
ReferenceGRCh38 38.1/142
Chromosome2
Position47161737
GeneCALM2
is asnp
is mentioned by
dbSNPrs398124649
ebirs398124649
HLIrs398124649
Exacrs398124649
Varsomers398124649
Maprs398124649
PheGenIrs398124649
hapmaprs398124649
1000 genomesrs398124649
hgdprs398124649
ensemblrs398124649
gopubmedrs398124649
geneviewrs398124649
scholarrs398124649
googlers398124649
pharmgkbrs398124649
gwascentralrs398124649
openSNPrs398124649
23andMers398124649
23andMe allrs398124649
SNP Nexus

SNPshotrs398124649
SNPdbers398124649
MSV3drs398124649
GWAS Ctlgrs398124649
Max Magnitude0
ClinVar
Risk rs398124649(C;C)
Alt rs398124649(C;C)
Reference rs398124649(A;A)
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.47388876T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000143840.1, RCV000162070.2,