rs199473659

Orientation

plus

Stabilized

plus

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

Make rs199473659(C;T)

Make rs199473659(T;T)

Reference

GRCh38 38.1/142

Chromosome

17

Position

70176090

Gene

KCNJ2

is a	snp
is	mentioned by
dbSNP	rs199473659
dbSNP (classic)	rs199473659
ClinGen	rs199473659
ebi	rs199473659
HLI	rs199473659
Exac	rs199473659
Gnomad	rs199473659
Varsome	rs199473659
LitVar	rs199473659
Map	rs199473659
PheGenI	rs199473659
Biobank	rs199473659
1000 genomes	rs199473659
hgdp	rs199473659
ensembl	rs199473659
geneview	rs199473659
scholar	rs199473659
google	rs199473659
pharmgkb	rs199473659
gwascentral	rs199473659
openSNP	rs199473659
23andMe	rs199473659
SNPshot	rs199473659
SNPdbe	rs199473659
MSV3d	rs199473659
GWAS Ctlg	rs199473659

Max Magnitude

0

ClinVar
Risk	rs199473659(T;T)
Alt	rs199473659(T;T)
Reference	Rs199473659(C;C)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNJ2
CLNDBN	Congenital long QT syndrome
Reversed	0
HGVS	NC_000017.10:g.68172231C>T
CLNSRC	ClinVar
CLNACC	RCV000058291.3,