rs180843436

Orientation

plus

Stabilized

plus

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

Make rs180843436(A;A)

Make rs180843436(A;G)

Reference

GRCh38 38.1/142

Chromosome

4

Position

113360849

Gene

ANK2

is a	snp
is	mentioned by
dbSNP	rs180843436
dbSNP (classic)	rs180843436
ClinGen	rs180843436
ebi	rs180843436
HLI	rs180843436
Exac	rs180843436
Gnomad	rs180843436
Varsome	rs180843436
LitVar	rs180843436
Map	rs180843436
PheGenI	rs180843436
Biobank	rs180843436
1000 genomes	rs180843436
hgdp	rs180843436
ensembl	rs180843436
geneview	rs180843436
scholar	rs180843436
google	rs180843436
pharmgkb	rs180843436
gwascentral	rs180843436
openSNP	rs180843436
23andMe	rs180843436
SNPshot	rs180843436
SNPdbe	rs180843436
MSV3d	rs180843436
GWAS Ctlg	rs180843436

Max Magnitude

0

ClinVar
Risk	rs180843436(A;A)
Alt	rs180843436(A;A)
Reference	Rs180843436(G;G)
Significance	Probable-Pathogenic
Disease	Congenital long QT syndrome Ventricular tachycardia not specified
Variation	info
Gene	ANK2
CLNDBN	Congenital long QT syndrome Ventricular tachycardia, catecholaminergic polymorphic, 1 not specified
Reversed	0
HGVS	NC_000004.11:g.114282005G>A
CLNSRC	Cardiovascular Biomedical Research Unit ClinVar
CLNACC	RCV000058340.3, RCV000143869.1, RCV000375362.1,