rs796052198

Orientation

plus

Stabilized

plus

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

Make rs796052198(C;C)

Make rs796052198(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

4

Position

113356741

Gene

ANK2

is a	snp
is	mentioned by
dbSNP	rs796052198
dbSNP (classic)	rs796052198
ClinGen	rs796052198
ebi	rs796052198
HLI	rs796052198
Exac	rs796052198
Gnomad	rs796052198
Varsome	rs796052198
LitVar	rs796052198
Map	rs796052198
PheGenI	rs796052198
Biobank	rs796052198
1000 genomes	rs796052198
hgdp	rs796052198
ensembl	rs796052198
geneview	rs796052198
scholar	rs796052198
google	rs796052198
pharmgkb	rs796052198
gwascentral	rs796052198
openSNP	rs796052198
23andMe	rs796052198
SNPshot	rs796052198
SNPdbe	rs796052198
MSV3d	rs796052198
GWAS Ctlg	rs796052198

Max Magnitude

0

ClinVar
Risk	rs796052198(C;C)
Alt	rs796052198(C;C)
Reference	Rs796052198(T;T)
Significance	Probable-Pathogenic
Disease	Long QT syndrome
Variation	info
Gene	ANK2
CLNDBN	Long QT syndrome
Reversed	0
HGVS	NC_000004.11:g.114277897T>C
CLNSRC
CLNACC	RCV000190221.1,