rs199473380

Orientation

plus

Stabilized

plus

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

Make rs199473380(G;T)

Make rs199473380(T;T)

Reference

GRCh38 38.1/142

Chromosome

17

Position

70175500

Gene

KCNJ2

is a	snp
is	mentioned by
dbSNP	rs199473380
dbSNP (classic)	rs199473380
ClinGen	rs199473380
ebi	rs199473380
HLI	rs199473380
Exac	rs199473380
Gnomad	rs199473380
Varsome	rs199473380
LitVar	rs199473380
Map	rs199473380
PheGenI	rs199473380
Biobank	rs199473380
1000 genomes	rs199473380
hgdp	rs199473380
ensembl	rs199473380
geneview	rs199473380
scholar	rs199473380
google	rs199473380
pharmgkb	rs199473380
gwascentral	rs199473380
openSNP	rs199473380
23andMe	rs199473380
SNPshot	rs199473380
SNPdbe	rs199473380
MSV3d	rs199473380
GWAS Ctlg	rs199473380

Max Magnitude

0

ClinVar
Risk	rs199473380(T;T)
Alt	rs199473380(T;T)
Reference	Rs199473380(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.68171641G>T
CLNSRC	ClinVar
CLNACC	RCV000058317.3,