rs199473378

Orientation

plus

Stabilized

plus

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

Make rs199473378(A;A)

Make rs199473378(A;G)

Reference

GRCh38 38.1/142

Chromosome

17

Position

70175469

Gene

KCNJ2

is a	snp
is	mentioned by
dbSNP	rs199473378
dbSNP (classic)	rs199473378
ClinGen	rs199473378
ebi	rs199473378
HLI	rs199473378
Exac	rs199473378
Gnomad	rs199473378
Varsome	rs199473378
LitVar	rs199473378
Map	rs199473378
PheGenI	rs199473378
Biobank	rs199473378
1000 genomes	rs199473378
hgdp	rs199473378
ensembl	rs199473378
geneview	rs199473378
scholar	rs199473378
google	rs199473378
pharmgkb	rs199473378
gwascentral	rs199473378
openSNP	rs199473378
23andMe	rs199473378
SNPshot	rs199473378
SNPdbe	rs199473378
MSV3d	rs199473378
GWAS Ctlg	rs199473378

Max Magnitude

0

ClinVar
Risk	rs199473378(A;A)
Alt	rs199473378(A;A)
Reference	Rs199473378(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.68171610G>A
CLNSRC	ClinVar
CLNACC	RCV000058311.3,