rs199473376

Orientation

plus

Stabilized

plus

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

Make rs199473376(C;T)

Make rs199473376(T;T)

Reference

GRCh38 38.1/142

Chromosome

17

Position

70175446

Gene

KCNJ2

is a	snp
is	mentioned by
dbSNP	rs199473376
dbSNP (classic)	rs199473376
ClinGen	rs199473376
ebi	rs199473376
HLI	rs199473376
Exac	rs199473376
Gnomad	rs199473376
Varsome	rs199473376
LitVar	rs199473376
Map	rs199473376
PheGenI	rs199473376
Biobank	rs199473376
1000 genomes	rs199473376
hgdp	rs199473376
ensembl	rs199473376
geneview	rs199473376
scholar	rs199473376
google	rs199473376
pharmgkb	rs199473376
gwascentral	rs199473376
openSNP	rs199473376
23andMe	rs199473376
SNPshot	rs199473376
SNPdbe	rs199473376
MSV3d	rs199473376
GWAS Ctlg	rs199473376

Max Magnitude

0

ClinVar
Risk	rs199473376(T;T)
Alt	rs199473376(T;T)
Reference	Rs199473376(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.68171587C>T
CLNSRC	ClinVar
CLNACC	RCV000058310.3,