rs398124649

Orientation

minus

Stabilized

minus

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

Make rs398124649(A;C)

Make rs398124649(C;C)

Reference

GRCh38 38.1/142

Chromosome

2

Position

47161737

Gene

CALM2

is a	snp
is	mentioned by
dbSNP	rs398124649
dbSNP (classic)	rs398124649
ClinGen	rs398124649
ebi	rs398124649
HLI	rs398124649
Exac	rs398124649
Gnomad	rs398124649
Varsome	rs398124649
LitVar	rs398124649
Map	rs398124649
PheGenI	rs398124649
Biobank	rs398124649
1000 genomes	rs398124649
hgdp	rs398124649
ensembl	rs398124649
geneview	rs398124649
scholar	rs398124649
google	rs398124649
pharmgkb	rs398124649
gwascentral	rs398124649
openSNP	rs398124649
23andMe	rs398124649
SNPshot	rs398124649
SNPdbe	rs398124649
MSV3d	rs398124649
GWAS Ctlg	rs398124649

Max Magnitude

0

ClinVar
Risk	rs398124649(C;C)
Alt	rs398124649(C;C)
Reference	Rs398124649(A;A)
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.47388876T>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000143840.1, RCV000162070.3,