rs199473390

Orientation

plus

Stabilized

plus

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

Make rs199473390(G;T)

Make rs199473390(T;T)

Reference

GRCh38 38.1/142

Chromosome

17

Position

70176304

Gene

KCNJ2

is a	snp
is	mentioned by
dbSNP	rs199473390
dbSNP (classic)	rs199473390
ClinGen	rs199473390
ebi	rs199473390
HLI	rs199473390
Exac	rs199473390
Gnomad	rs199473390
Varsome	rs199473390
LitVar	rs199473390
Map	rs199473390
PheGenI	rs199473390
Biobank	rs199473390
1000 genomes	rs199473390
hgdp	rs199473390
ensembl	rs199473390
geneview	rs199473390
scholar	rs199473390
google	rs199473390
pharmgkb	rs199473390
gwascentral	rs199473390
openSNP	rs199473390
23andMe	rs199473390
SNPshot	rs199473390
SNPdbe	rs199473390
MSV3d	rs199473390
GWAS Ctlg	rs199473390

Max Magnitude

0

ClinVar
Risk	rs199473390(A;A) rs199473390(C;C) rs199473390(T;T)
Alt	rs199473390(A;A) rs199473390(C;C) rs199473390(T;T)
Reference	Rs199473390(G;G)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNJ2
CLNDBN	Congenital long QT syndrome
Reversed	0
HGVS	NC_000017.10:g.68172445G>T
CLNSRC	ClinVar
CLNACC	RCV000058292.3,