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rs267607277

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607277(A;G)
Make rs267607277(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position90404386
GeneCALM1
is asnp
is mentioned by
dbSNPrs267607277
ebirs267607277
HLIrs267607277
Exacrs267607277
Varsomers267607277
Maprs267607277
PheGenIrs267607277
hapmaprs267607277
1000 genomesrs267607277
hgdprs267607277
ensemblrs267607277
gopubmedrs267607277
geneviewrs267607277
scholarrs267607277
googlers267607277
pharmgkbrs267607277
gwascentralrs267607277
openSNPrs267607277
23andMers267607277
23andMe allrs267607277
SNP Nexus

SNPshotrs267607277
SNPdbers267607277
MSV3drs267607277
GWAS Ctlgrs267607277
Max Magnitude0
ClinVar
Risk rs267607277(G;G)
Alt rs267607277(G;G)
Reference rs267607277(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.90870730A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000032977.29, RCV000157134.1,