rs199473386

Orientation

plus

Stabilized

plus

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

Make rs199473386(A;A)

Make rs199473386(A;G)

Reference

GRCh38 38.1/142

Chromosome

17

Position

70175946

Gene

KCNJ2

is a	snp
is	mentioned by
dbSNP	rs199473386
dbSNP (classic)	rs199473386
ClinGen	rs199473386
ebi	rs199473386
HLI	rs199473386
Exac	rs199473386
Gnomad	rs199473386
Varsome	rs199473386
LitVar	rs199473386
Map	rs199473386
PheGenI	rs199473386
Biobank	rs199473386
1000 genomes	rs199473386
hgdp	rs199473386
ensembl	rs199473386
geneview	rs199473386
scholar	rs199473386
google	rs199473386
pharmgkb	rs199473386
gwascentral	rs199473386
openSNP	rs199473386
23andMe	rs199473386
SNPshot	rs199473386
SNPdbe	rs199473386
MSV3d	rs199473386
GWAS Ctlg	rs199473386

Max Magnitude

0

ClinVar
Risk	rs199473386(A;A)
Alt	rs199473386(A;A)
Reference	Rs199473386(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.68172087G>A
CLNSRC	ClinVar
CLNACC	RCV000058334.3,