rs199472882

Orientation

minus

Stabilized

minus

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

Make rs199472882(C;T)

Make rs199472882(T;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150958086

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199472882
dbSNP (classic)	rs199472882
ClinGen	rs199472882
ebi	rs199472882
HLI	rs199472882
Exac	rs199472882
Gnomad	rs199472882
Varsome	rs199472882
LitVar	rs199472882
Map	rs199472882
PheGenI	rs199472882
Biobank	rs199472882
1000 genomes	rs199472882
hgdp	rs199472882
ensembl	rs199472882
geneview	rs199472882
scholar	rs199472882
google	rs199472882
pharmgkb	rs199472882
gwascentral	rs199472882
openSNP	rs199472882
23andMe	rs199472882
SNPshot	rs199472882
SNPdbe	rs199472882
MSV3d	rs199472882
GWAS Ctlg	rs199472882

Max Magnitude

0

ClinVar
Risk	rs199472882(T;T)
Alt	rs199472882(T;T)
Reference	Rs199472882(C;C)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150655174G>A
CLNSRC	ClinVar
CLNACC	RCV000058269.3,