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rs267607276

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607276(A;T)
Make rs267607276(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position90401385
GeneCALM1
is asnp
is mentioned by
dbSNPrs267607276
ebirs267607276
HLIrs267607276
Exacrs267607276
Varsomers267607276
Maprs267607276
PheGenIrs267607276
hapmaprs267607276
1000 genomesrs267607276
hgdprs267607276
ensemblrs267607276
gopubmedrs267607276
geneviewrs267607276
scholarrs267607276
googlers267607276
pharmgkbrs267607276
gwascentralrs267607276
openSNPrs267607276
23andMers267607276
23andMe allrs267607276
SNP Nexus

SNPshotrs267607276
SNPdbers267607276
MSV3drs267607276
GWAS Ctlgrs267607276
Max Magnitude0
ClinVar
Risk rs267607276(T;T)
Alt rs267607276(T;T)
Reference rs267607276(A;A)
Significance Pathogenic
Disease Ventricular tachycardia Ventricular tachycardia
Variation info
Gene CALM1
CLNDBN Ventricular tachycardia, catecholaminergic polymorphic, 4 Ventricular tachycardia, catecholaminergic polymorphic, 1
Reversed 0
HGVS NC_000014.8:g.90867729A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000032976.29, RCV000157133.1,