rs199473368

Orientation

plus

Stabilized

plus

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

Make rs199473368(A;A)

Make rs199473368(A;G)

Reference

GRCh38 38.1/142

Chromosome

17

Position

70175239

Gene

KCNJ2

is a	snp
is	mentioned by
dbSNP	rs199473368
dbSNP (classic)	rs199473368
ClinGen	rs199473368
ebi	rs199473368
HLI	rs199473368
Exac	rs199473368
Gnomad	rs199473368
Varsome	rs199473368
LitVar	rs199473368
Map	rs199473368
PheGenI	rs199473368
Biobank	rs199473368
1000 genomes	rs199473368
hgdp	rs199473368
ensembl	rs199473368
geneview	rs199473368
scholar	rs199473368
google	rs199473368
pharmgkb	rs199473368
gwascentral	rs199473368
openSNP	rs199473368
23andMe	rs199473368
SNPshot	rs199473368
SNPdbe	rs199473368
MSV3d	rs199473368
GWAS Ctlg	rs199473368

Max Magnitude

0

ClinVar
Risk	rs199473368(A;A)
Alt	rs199473368(A;A)
Reference	Rs199473368(G;G)
Significance	Pathogenic
Disease	Congenital long QT syndrome not provided
Variation	info
Gene	KCNJ2
CLNDBN	Congenital long QT syndrome not provided
Reversed	0
HGVS	NC_000017.10:g.68171380G>A
CLNSRC	ClinVar
CLNACC	RCV000058295.3, RCV000170972.3,