rs199473652

Orientation

plus

Stabilized

plus

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

Make rs199473652(A;G)

Make rs199473652(G;G)

Reference

GRCh38 38.1/142

Chromosome

17

Position

70175259

Gene

KCNJ2

is a	snp
is	mentioned by
dbSNP	rs199473652
dbSNP (classic)	rs199473652
ClinGen	rs199473652
ebi	rs199473652
HLI	rs199473652
Exac	rs199473652
Gnomad	rs199473652
Varsome	rs199473652
LitVar	rs199473652
Map	rs199473652
PheGenI	rs199473652
Biobank	rs199473652
1000 genomes	rs199473652
hgdp	rs199473652
ensembl	rs199473652
geneview	rs199473652
scholar	rs199473652
google	rs199473652
pharmgkb	rs199473652
gwascentral	rs199473652
openSNP	rs199473652
23andMe	rs199473652
SNPshot	rs199473652
SNPdbe	rs199473652
MSV3d	rs199473652
GWAS Ctlg	rs199473652

Max Magnitude

0

ClinVar
Risk	rs199473652(G;G)
Alt	rs199473652(G;G)
Reference	Rs199473652(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.68171400A>G
CLNSRC	ClinVar
CLNACC	RCV000058299.3,