rs796052197

Orientation

plus

Stabilized

plus

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

Make rs796052197(C;C)

Make rs796052197(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

4

Position

113354767

Gene

ANK2

is a	snp
is	mentioned by
dbSNP	rs796052197
dbSNP (classic)	rs796052197
ClinGen	rs796052197
ebi	rs796052197
HLI	rs796052197
Exac	rs796052197
Gnomad	rs796052197
Varsome	rs796052197
LitVar	rs796052197
Map	rs796052197
PheGenI	rs796052197
Biobank	rs796052197
1000 genomes	rs796052197
hgdp	rs796052197
ensembl	rs796052197
geneview	rs796052197
scholar	rs796052197
google	rs796052197
pharmgkb	rs796052197
gwascentral	rs796052197
openSNP	rs796052197
23andMe	rs796052197
SNPshot	rs796052197
SNPdbe	rs796052197
MSV3d	rs796052197
GWAS Ctlg	rs796052197

Max Magnitude

0

ClinVar
Risk	rs796052197(C;C)
Alt	rs796052197(C;C)
Reference	Rs796052197(T;T)
Significance	Probable-Pathogenic
Disease	Long QT syndrome
Variation	info
Gene	ANK2
CLNDBN	Long QT syndrome
Reversed	0
HGVS	NC_000004.11:g.114275923T>C
CLNSRC
CLNACC	RCV000190220.1,