rs199473035

Orientation

minus

Stabilized

minus

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

Make rs199473035(C;T)

Make rs199473035(T;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150945388

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473035
dbSNP (classic)	rs199473035
ClinGen	rs199473035
ebi	rs199473035
HLI	rs199473035
Exac	rs199473035
Gnomad	rs199473035
Varsome	rs199473035
LitVar	rs199473035
Map	rs199473035
PheGenI	rs199473035
Biobank	rs199473035
1000 genomes	rs199473035
hgdp	rs199473035
ensembl	rs199473035
geneview	rs199473035
scholar	rs199473035
google	rs199473035
pharmgkb	rs199473035
gwascentral	rs199473035
openSNP	rs199473035
23andMe	rs199473035
SNPshot	rs199473035
SNPdbe	rs199473035
MSV3d	rs199473035
GWAS Ctlg	rs199473035

Max Magnitude

0

ClinVar
Risk	rs199473035(T;T)
Alt	rs199473035(T;T)
Reference	Rs199473035(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.150642476G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058226.3,