rs199472889

Orientation

minus

Stabilized

minus

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

Make rs199472889(A;T)

Make rs199472889(T;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150957394

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199472889
dbSNP (classic)	rs199472889
ClinGen	rs199472889
ebi	rs199472889
HLI	rs199472889
Exac	rs199472889
Gnomad	rs199472889
Varsome	rs199472889
LitVar	rs199472889
Map	rs199472889
PheGenI	rs199472889
Biobank	rs199472889
1000 genomes	rs199472889
hgdp	rs199472889
ensembl	rs199472889
geneview	rs199472889
scholar	rs199472889
google	rs199472889
pharmgkb	rs199472889
gwascentral	rs199472889
openSNP	rs199472889
23andMe	rs199472889
SNPshot	rs199472889
SNPdbe	rs199472889
MSV3d	rs199472889
GWAS Ctlg	rs199472889

Max Magnitude

0

ClinVar
Risk	rs199472889(C;C) rs199472889(T;T)
Alt	rs199472889(C;C) rs199472889(T;T)
Reference	Rs199472889(A;A)
Significance	Untested
Disease	Acquired long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Acquired long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150654482T>A
CLNSRC	ClinVar
CLNACC	RCV000057869.3,