rs199473655

Orientation

plus

Stabilized

plus

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

Make rs199473655(C;T)

Make rs199473655(T;T)

Reference

GRCh38 38.1/142

Chromosome

17

Position

70175614

Gene

KCNJ2

is a	snp
is	mentioned by
dbSNP	rs199473655
dbSNP (classic)	rs199473655
ClinGen	rs199473655
ebi	rs199473655
HLI	rs199473655
Exac	rs199473655
Gnomad	rs199473655
Varsome	rs199473655
LitVar	rs199473655
Map	rs199473655
PheGenI	rs199473655
Biobank	rs199473655
1000 genomes	rs199473655
hgdp	rs199473655
ensembl	rs199473655
geneview	rs199473655
scholar	rs199473655
google	rs199473655
pharmgkb	rs199473655
gwascentral	rs199473655
openSNP	rs199473655
23andMe	rs199473655
SNPshot	rs199473655
SNPdbe	rs199473655
MSV3d	rs199473655
GWAS Ctlg	rs199473655

Max Magnitude

0

ClinVar
Risk	rs199473655(T;T)
Alt	rs199473655(T;T)
Reference	Rs199473655(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.68171755C>T
CLNSRC	ClinVar
CLNACC	RCV000058322.3,