rs199473388

Orientation

plus

Stabilized

plus

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

Make rs199473388(C;T)

Make rs199473388(T;T)

Reference

GRCh38 38.1/142

Chromosome

17

Position

70175965

Gene

KCNJ2

is a	snp
is	mentioned by
dbSNP	rs199473388
dbSNP (classic)	rs199473388
ClinGen	rs199473388
ebi	rs199473388
HLI	rs199473388
Exac	rs199473388
Gnomad	rs199473388
Varsome	rs199473388
LitVar	rs199473388
Map	rs199473388
PheGenI	rs199473388
Biobank	rs199473388
1000 genomes	rs199473388
hgdp	rs199473388
ensembl	rs199473388
geneview	rs199473388
scholar	rs199473388
google	rs199473388
pharmgkb	rs199473388
gwascentral	rs199473388
openSNP	rs199473388
23andMe	rs199473388
SNPshot	rs199473388
SNPdbe	rs199473388
MSV3d	rs199473388
GWAS Ctlg	rs199473388

Max Magnitude

0

ClinVar
Risk	rs199473388(T;T)
Alt	rs199473388(T;T)
Reference	Rs199473388(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.68172106C>T
CLNSRC	ClinVar
CLNACC	RCV000058338.3,