rs199473372

Orientation

plus

Stabilized

plus

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

Make rs199473372(G;T)

Make rs199473372(T;T)

Reference

GRCh38 38.1/142

Chromosome

17

Position

70175271

Gene

KCNJ2

is a	snp
is	mentioned by
dbSNP	rs199473372
dbSNP (classic)	rs199473372
ClinGen	rs199473372
ebi	rs199473372
HLI	rs199473372
Exac	rs199473372
Gnomad	rs199473372
Varsome	rs199473372
LitVar	rs199473372
Map	rs199473372
PheGenI	rs199473372
Biobank	rs199473372
1000 genomes	rs199473372
hgdp	rs199473372
ensembl	rs199473372
geneview	rs199473372
scholar	rs199473372
google	rs199473372
pharmgkb	rs199473372
gwascentral	rs199473372
openSNP	rs199473372
23andMe	rs199473372
SNPshot	rs199473372
SNPdbe	rs199473372
MSV3d	rs199473372
GWAS Ctlg	rs199473372

Max Magnitude

0

ClinVar
Risk	rs199473372(T;T)
Alt	rs199473372(T;T)
Reference	Rs199473372(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.68171412G>T
CLNSRC	ClinVar
CLNACC	RCV000058303.3,