rs267607276

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs267607276(A;T)

Make rs267607276(T;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

90401385

Gene

CALM1

is a	snp
is	mentioned by
dbSNP	rs267607276
dbSNP (classic)	rs267607276
ClinGen	rs267607276
ebi	rs267607276
HLI	rs267607276
Exac	rs267607276
Gnomad	rs267607276
Varsome	rs267607276
LitVar	rs267607276
Map	rs267607276
PheGenI	rs267607276
Biobank	rs267607276
1000 genomes	rs267607276
hgdp	rs267607276
ensembl	rs267607276
geneview	rs267607276
scholar	rs267607276
google	rs267607276
pharmgkb	rs267607276
gwascentral	rs267607276
openSNP	rs267607276
23andMe	rs267607276
SNPshot	rs267607276
SNPdbe	rs267607276
MSV3d	rs267607276
GWAS Ctlg	rs267607276

Max Magnitude

0

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 UniProtKB (protein)
CLNACC	RCV000032976.29, RCV000157133.1,