rs199473370

Orientation

plus

Stabilized

plus

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

Make rs199473370(A;G)

Make rs199473370(G;G)

Reference

GRCh38 38.1/142

Chromosome

17

Position

70175262

Gene

KCNJ2

is a	snp
is	mentioned by
dbSNP	rs199473370
dbSNP (classic)	rs199473370
ClinGen	rs199473370
ebi	rs199473370
HLI	rs199473370
Exac	rs199473370
Gnomad	rs199473370
Varsome	rs199473370
LitVar	rs199473370
Map	rs199473370
PheGenI	rs199473370
Biobank	rs199473370
1000 genomes	rs199473370
hgdp	rs199473370
ensembl	rs199473370
geneview	rs199473370
scholar	rs199473370
google	rs199473370
pharmgkb	rs199473370
gwascentral	rs199473370
openSNP	rs199473370
23andMe	rs199473370
SNPshot	rs199473370
SNPdbe	rs199473370
MSV3d	rs199473370
GWAS Ctlg	rs199473370

Max Magnitude

0

ClinVar
Risk	rs199473370(G;G)
Alt	rs199473370(G;G)
Reference	Rs199473370(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.68171403A>G
CLNSRC	ClinVar
CLNACC	RCV000058300.3,