rs730882252

Orientation

plus

Stabilized

plus

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

Make rs730882252(A;G)

Make rs730882252(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

90404482

Gene

CALM1

is a	snp
is	mentioned by
dbSNP	rs730882252
dbSNP (classic)	rs730882252
ClinGen	rs730882252
ebi	rs730882252
HLI	rs730882252
Exac	rs730882252
Gnomad	rs730882252
Varsome	rs730882252
LitVar	rs730882252
Map	rs730882252
PheGenI	rs730882252
Biobank	rs730882252
1000 genomes	rs730882252
hgdp	rs730882252
ensembl	rs730882252
geneview	rs730882252
scholar	rs730882252
google	rs730882252
pharmgkb	rs730882252
gwascentral	rs730882252
openSNP	rs730882252
23andMe	rs730882252
SNPshot	rs730882252
SNPdbe	rs730882252
MSV3d	rs730882252
GWAS Ctlg	rs730882252

Max Magnitude

0

ClinVar
Risk	rs730882252(G;G)
Alt	rs730882252(G;G)
Reference	Rs730882252(A;A)
Significance	Pathogenic
Disease	Long QT syndrome 14
Variation	info
Gene	CALM1
CLNDBN	Long QT syndrome 14
Reversed	0
HGVS	NC_000014.8:g.90870826A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000162062.4,