rs199473385

Orientation

plus

Stabilized

plus

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

Make rs199473385(C;C)

Make rs199473385(C;G)

Reference

GRCh38 38.1/142

Chromosome

17

Position

70175818

Gene

KCNJ2

is a	snp
is	mentioned by
dbSNP	rs199473385
dbSNP (classic)	rs199473385
ClinGen	rs199473385
ebi	rs199473385
HLI	rs199473385
Exac	rs199473385
Gnomad	rs199473385
Varsome	rs199473385
LitVar	rs199473385
Map	rs199473385
PheGenI	rs199473385
Biobank	rs199473385
1000 genomes	rs199473385
hgdp	rs199473385
ensembl	rs199473385
geneview	rs199473385
scholar	rs199473385
google	rs199473385
pharmgkb	rs199473385
gwascentral	rs199473385
openSNP	rs199473385
23andMe	rs199473385
SNPshot	rs199473385
SNPdbe	rs199473385
MSV3d	rs199473385
GWAS Ctlg	rs199473385

Max Magnitude

0

ClinVar
Risk	rs199473385(C;C)
Alt	rs199473385(C;C)
Reference	Rs199473385(G;G)
Significance	Pathogenic
Disease	Congenital long QT syndrome not provided
Variation	info
Gene	KCNJ2
CLNDBN	Congenital long QT syndrome not provided
Reversed	0
HGVS	NC_000017.10:g.68171959G>C
CLNSRC	ClinVar
CLNACC	RCV000058329.3, RCV000170984.2,