rs199472858

Orientation

minus

Stabilized

minus

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

Make rs199472858(A;A)

Make rs199472858(A;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150959727

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199472858
dbSNP (classic)	rs199472858
ClinGen	rs199472858
ebi	rs199472858
HLI	rs199472858
Exac	rs199472858
Gnomad	rs199472858
Varsome	rs199472858
LitVar	rs199472858
Map	rs199472858
PheGenI	rs199472858
Biobank	rs199472858
1000 genomes	rs199472858
hgdp	rs199472858
ensembl	rs199472858
geneview	rs199472858
scholar	rs199472858
google	rs199472858
pharmgkb	rs199472858
gwascentral	rs199472858
openSNP	rs199472858
23andMe	rs199472858
SNPshot	rs199472858
SNPdbe	rs199472858
MSV3d	rs199472858
GWAS Ctlg	rs199472858

Max Magnitude

0

ClinVar
Risk	rs199472858(A;A)
Alt	rs199472858(A;A)
Reference	Rs199472858(T;T)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150656815A>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058206.3,