rs199473382

Orientation

plus

Stabilized

plus

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

Make rs199473382(A;G)

Make rs199473382(G;G)

Reference

GRCh38 38.1/142

Chromosome

17

Position

70175613

Gene

KCNJ2

is a	snp
is	mentioned by
dbSNP	rs199473382
dbSNP (classic)	rs199473382
ClinGen	rs199473382
ebi	rs199473382
HLI	rs199473382
Exac	rs199473382
Gnomad	rs199473382
Varsome	rs199473382
LitVar	rs199473382
Map	rs199473382
PheGenI	rs199473382
Biobank	rs199473382
1000 genomes	rs199473382
hgdp	rs199473382
ensembl	rs199473382
geneview	rs199473382
scholar	rs199473382
google	rs199473382
pharmgkb	rs199473382
gwascentral	rs199473382
openSNP	rs199473382
23andMe	rs199473382
SNPshot	rs199473382
SNPdbe	rs199473382
MSV3d	rs199473382
GWAS Ctlg	rs199473382

Max Magnitude

0

ClinVar
Risk	rs199473382(G;G)
Alt	rs199473382(G;G)
Reference	Rs199473382(A;A)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNJ2
CLNDBN	Congenital long QT syndrome
Reversed	0
HGVS	NC_000017.10:g.68171754A>G
CLNSRC	ClinVar
CLNACC	RCV000058321.3,