rs148654834

Orientation

plus

Stabilized

plus

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

Make rs148654834(C;C)

Make rs148654834(C;G)

Reference

GRCh38 38.1/142

Chromosome

4

Position

113369711

Gene

ANK2

is a	snp
is	mentioned by
dbSNP	rs148654834
dbSNP (classic)	rs148654834
ClinGen	rs148654834
ebi	rs148654834
HLI	rs148654834
Exac	rs148654834
Gnomad	rs148654834
Varsome	rs148654834
LitVar	rs148654834
Map	rs148654834
PheGenI	rs148654834
Biobank	rs148654834
1000 genomes	rs148654834
hgdp	rs148654834
ensembl	rs148654834
geneview	rs148654834
scholar	rs148654834
google	rs148654834
pharmgkb	rs148654834
gwascentral	rs148654834
openSNP	rs148654834
23andMe	rs148654834
SNPshot	rs148654834
SNPdbe	rs148654834
MSV3d	rs148654834
GWAS Ctlg	rs148654834

Max Magnitude

0

ClinVar
Risk	rs148654834(C;C)
Alt	rs148654834(C;C)
Reference	Rs148654834(G;G)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	ANK2
CLNDBN	Congenital long QT syndrome
Reversed	0
HGVS	NC_000004.11:g.114290867G>C
CLNSRC	Cardiovascular Biomedical Research Unit ClinVar
CLNACC	RCV000058348.3,