rs199473375

Orientation

plus

Stabilized

plus

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

Make rs199473375(G;G)

Make rs199473375(G;T)

Reference

GRCh38 38.1/142

Chromosome

17

Position

70175407

Gene

KCNJ2

is a	snp
is	mentioned by
dbSNP	rs199473375
dbSNP (classic)	rs199473375
ClinGen	rs199473375
ebi	rs199473375
HLI	rs199473375
Exac	rs199473375
Gnomad	rs199473375
Varsome	rs199473375
LitVar	rs199473375
Map	rs199473375
PheGenI	rs199473375
Biobank	rs199473375
1000 genomes	rs199473375
hgdp	rs199473375
ensembl	rs199473375
geneview	rs199473375
scholar	rs199473375
google	rs199473375
pharmgkb	rs199473375
gwascentral	rs199473375
openSNP	rs199473375
23andMe	rs199473375
SNPshot	rs199473375
SNPdbe	rs199473375
MSV3d	rs199473375
GWAS Ctlg	rs199473375

Max Magnitude

0

ClinVar
Risk	rs199473375(G;G)
Alt	rs199473375(G;G)
Reference	Rs199473375(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.68171548T>G
CLNSRC	ClinVar
CLNACC	RCV000058309.3,