rs199473654

Orientation

plus

Stabilized

plus

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

Make rs199473654(A;A)

Make rs199473654(A;G)

Reference

GRCh38 38.1/142

Chromosome

17

Position

70175475

Gene

KCNJ2

is a	snp
is	mentioned by
dbSNP	rs199473654
dbSNP (classic)	rs199473654
ClinGen	rs199473654
ebi	rs199473654
HLI	rs199473654
Exac	rs199473654
Gnomad	rs199473654
Varsome	rs199473654
LitVar	rs199473654
Map	rs199473654
PheGenI	rs199473654
Biobank	rs199473654
1000 genomes	rs199473654
hgdp	rs199473654
ensembl	rs199473654
geneview	rs199473654
scholar	rs199473654
google	rs199473654
pharmgkb	rs199473654
gwascentral	rs199473654
openSNP	rs199473654
23andMe	rs199473654
SNPshot	rs199473654
SNPdbe	rs199473654
MSV3d	rs199473654
GWAS Ctlg	rs199473654

Max Magnitude

0

ClinVar
Risk	rs199473654(A;A)
Alt	rs199473654(A;A)
Reference	Rs199473654(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.68171616G>A
CLNSRC	ClinVar
CLNACC	RCV000058314.3,