rs45570339

Orientation

plus

Stabilized

plus

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

Make rs45570339(C;G)

Make rs45570339(G;G)

Reference

GRCh38 38.1/142

Chromosome

4

Position

113363442

Gene

ANK2

is a	snp
is	mentioned by
dbSNP	rs45570339
dbSNP (classic)	rs45570339
ClinGen	rs45570339
ebi	rs45570339
HLI	rs45570339
Exac	rs45570339
Gnomad	rs45570339
Varsome	rs45570339
LitVar	rs45570339
Map	rs45570339
PheGenI	rs45570339
Biobank	rs45570339
1000 genomes	rs45570339
hgdp	rs45570339
ensembl	rs45570339
geneview	rs45570339
scholar	rs45570339
google	rs45570339
pharmgkb	rs45570339
gwascentral	rs45570339
openSNP	rs45570339
23andMe	rs45570339
SNPshot	rs45570339
SNPdbe	rs45570339
MSV3d	rs45570339
GWAS Ctlg	rs45570339

Max Magnitude

0

ClinVar
Risk	rs45570339(G;G)
Alt	rs45570339(G;G)
Reference	Rs45570339(C;C)
Significance	Probable-non-pathogenic
Disease	Congenital long QT syndrome not specified Long QT syndrome
Variation	info
Gene	ANK2
CLNDBN	Congenital long QT syndrome not specified Long QT syndrome
Reversed	0
HGVS	NC_000004.11:g.114284598C>G
CLNSRC	Cardiovascular Biomedical Research Unit ClinVar
CLNACC	RCV000058342.3, RCV000170658.4, RCV000171796.2,