rs199473651

Orientation

plus

Stabilized

plus

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

Make rs199473651(G;G)

Make rs199473651(G;T)

Reference

GRCh38 38.1/142

Chromosome

17

Position

70175241

Gene

KCNJ2

is a	snp
is	mentioned by
dbSNP	rs199473651
dbSNP (classic)	rs199473651
ClinGen	rs199473651
ebi	rs199473651
HLI	rs199473651
Exac	rs199473651
Gnomad	rs199473651
Varsome	rs199473651
LitVar	rs199473651
Map	rs199473651
PheGenI	rs199473651
Biobank	rs199473651
1000 genomes	rs199473651
hgdp	rs199473651
ensembl	rs199473651
geneview	rs199473651
scholar	rs199473651
google	rs199473651
pharmgkb	rs199473651
gwascentral	rs199473651
openSNP	rs199473651
23andMe	rs199473651
SNPshot	rs199473651
SNPdbe	rs199473651
MSV3d	rs199473651
GWAS Ctlg	rs199473651

Max Magnitude

0

ClinVar
Risk	rs199473651(G;G)
Alt	rs199473651(G;G)
Reference	Rs199473651(T;T)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNJ2
CLNDBN	Congenital long QT syndrome
Reversed	0
HGVS	NC_000017.10:g.68171382T>G
CLNSRC	ClinVar
CLNACC	RCV000058296.3,