rs199472864

Orientation

minus

Stabilized

minus

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

Make rs199472864(C;T)

Make rs199472864(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150959622

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199472864
dbSNP (classic)	rs199472864
ClinGen	rs199472864
ebi	rs199472864
HLI	rs199472864
Exac	rs199472864
Gnomad	rs199472864
Varsome	rs199472864
LitVar	rs199472864
Map	rs199472864
PheGenI	rs199472864
Biobank	rs199472864
1000 genomes	rs199472864
hgdp	rs199472864
ensembl	rs199472864
geneview	rs199472864
scholar	rs199472864
google	rs199472864
pharmgkb	rs199472864
gwascentral	rs199472864
openSNP	rs199472864
23andMe	rs199472864
SNPshot	rs199472864
SNPdbe	rs199472864
MSV3d	rs199472864
GWAS Ctlg	rs199472864

Max Magnitude

0

ClinVar
Risk	rs199472864(T;T)
Alt	rs199472864(T;T)
Reference	Rs199472864(C;C)
Significance	Other
Disease	not provided Long QT syndrome not specified
Variation	info
Gene	KCNH2
CLNDBN	not provided Long QT syndrome not specified
Reversed	1
HGVS	NC_000007.13:g.150656710G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058233.3, RCV000148539.1, RCV000181756.2,