rs199473658

Orientation

plus

Stabilized

plus

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

Make rs199473658(A;A)

Make rs199473658(A;G)

Reference

GRCh38 38.1/142

Chromosome

17

Position

70175960

Gene

KCNJ2

is a	snp
is	mentioned by
dbSNP	rs199473658
dbSNP (classic)	rs199473658
ClinGen	rs199473658
ebi	rs199473658
HLI	rs199473658
Exac	rs199473658
Gnomad	rs199473658
Varsome	rs199473658
LitVar	rs199473658
Map	rs199473658
PheGenI	rs199473658
Biobank	rs199473658
1000 genomes	rs199473658
hgdp	rs199473658
ensembl	rs199473658
geneview	rs199473658
scholar	rs199473658
google	rs199473658
pharmgkb	rs199473658
gwascentral	rs199473658
openSNP	rs199473658
23andMe	rs199473658
SNPshot	rs199473658
SNPdbe	rs199473658
MSV3d	rs199473658
GWAS Ctlg	rs199473658

Max Magnitude

0

ClinVar
Risk	rs199473658(A;A)
Alt	rs199473658(A;A)
Reference	Rs199473658(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.68172101G>A
CLNSRC	ClinVar
CLNACC	RCV000058337.3,