rs137853228

Orientation

plus

Stabilized

plus

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

Make rs137853228(A;A)

Make rs137853228(A;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

50256729

Gene

GNAI2

is a	snp
is	mentioned by
dbSNP	rs137853228
dbSNP (classic)	rs137853228
ClinGen	rs137853228
ebi	rs137853228
HLI	rs137853228
Exac	rs137853228
Gnomad	rs137853228
Varsome	rs137853228
LitVar	rs137853228
Map	rs137853228
PheGenI	rs137853228
Biobank	rs137853228
1000 genomes	rs137853228
hgdp	rs137853228
ensembl	rs137853228
geneview	rs137853228
scholar	rs137853228
google	rs137853228
pharmgkb	rs137853228
gwascentral	rs137853228
openSNP	rs137853228
23andMe	rs137853228
SNPshot	rs137853228
SNPdbe	rs137853228
MSV3d	rs137853228
GWAS Ctlg	rs137853228

Max Magnitude

0

OMIM	139360
Desc
Variant	0004
Related	also

ClinVar
Risk	rs137853228(A;A)
Alt	rs137853228(A;A)
Reference	Rs137853228(T;T)
Significance	Pathogenic
Disease	Ventricular tachycardia
Variation	info
Gene	GNAI2
CLNDBN	Ventricular tachycardia, somatic
Reversed	0
HGVS	NC_000003.11:g.50294161T>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017257.4,