rs199473533

Orientation

minus

Stabilized

minus

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

Make rs199473533(A;T)

Make rs199473533(T;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150950384

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473533
dbSNP (classic)	rs199473533
ClinGen	rs199473533
ebi	rs199473533
HLI	rs199473533
Exac	rs199473533
Gnomad	rs199473533
Varsome	rs199473533
LitVar	rs199473533
Map	rs199473533
PheGenI	rs199473533
Biobank	rs199473533
1000 genomes	rs199473533
hgdp	rs199473533
ensembl	rs199473533
geneview	rs199473533
scholar	rs199473533
google	rs199473533
pharmgkb	rs199473533
gwascentral	rs199473533
openSNP	rs199473533
23andMe	rs199473533
SNPshot	rs199473533
SNPdbe	rs199473533
MSV3d	rs199473533
GWAS Ctlg	rs199473533

Max Magnitude

0

ClinVar
Risk	rs199473533(T;T)
Alt	rs199473533(T;T)
Reference	Rs199473533(A;A)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150647472T>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058093.3,