rs143228029

Orientation

plus

Stabilized

plus

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

Make rs143228029(A;A)

Make rs143228029(A;G)

Reference

GRCh38 38.1/142

Chromosome

4

Position

113365050

Gene

ANK2

is a	snp
is	mentioned by
dbSNP	rs143228029
dbSNP (classic)	rs143228029
ClinGen	rs143228029
ebi	rs143228029
HLI	rs143228029
Exac	rs143228029
Gnomad	rs143228029
Varsome	rs143228029
LitVar	rs143228029
Map	rs143228029
PheGenI	rs143228029
Biobank	rs143228029
1000 genomes	rs143228029
hgdp	rs143228029
ensembl	rs143228029
geneview	rs143228029
scholar	rs143228029
google	rs143228029
pharmgkb	rs143228029
gwascentral	rs143228029
openSNP	rs143228029
23andMe	rs143228029
SNPshot	rs143228029
SNPdbe	rs143228029
MSV3d	rs143228029
GWAS Ctlg	rs143228029

Max Magnitude

0

ClinVar
Risk	rs143228029(A;A)
Alt	rs143228029(A;A)
Reference	Rs143228029(G;G)
Significance	Untested
Disease	Congenital long QT syndrome Long QT syndrome
Variation	info
Gene	ANK2
CLNDBN	Congenital long QT syndrome Long QT syndrome
Reversed	0
HGVS	NC_000004.11:g.114286206G>A
CLNSRC	Cardiovascular Biomedical Research Unit ClinVar
CLNACC	RCV000058343.3, RCV000467680.1,