rs398124648

Orientation

minus

Stabilized

minus

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

Make rs398124648(G;G)

Make rs398124648(G;T)

Reference

GRCh38 38.1/142

Chromosome

2

Position

47161748

Gene

CALM2

is a	snp
is	mentioned by
dbSNP	rs398124648
dbSNP (classic)	rs398124648
ClinGen	rs398124648
ebi	rs398124648
HLI	rs398124648
Exac	rs398124648
Gnomad	rs398124648
Varsome	rs398124648
LitVar	rs398124648
Map	rs398124648
PheGenI	rs398124648
Biobank	rs398124648
1000 genomes	rs398124648
hgdp	rs398124648
ensembl	rs398124648
geneview	rs398124648
scholar	rs398124648
google	rs398124648
pharmgkb	rs398124648
gwascentral	rs398124648
openSNP	rs398124648
23andMe	rs398124648
SNPshot	rs398124648
SNPdbe	rs398124648
MSV3d	rs398124648
GWAS Ctlg	rs398124648

Max Magnitude

0

ClinVar
Risk	rs398124648(G;G)
Alt	rs398124648(G;G)
Reference	Rs398124648(T;T)
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.47388887A>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000143838.1, RCV000162069.3,