rs199472859

Orientation

minus

Stabilized

minus

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

Make rs199472859(C;C)

Make rs199472859(C;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150959722

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199472859
dbSNP (classic)	rs199472859
ClinGen	rs199472859
ebi	rs199472859
HLI	rs199472859
Exac	rs199472859
Gnomad	rs199472859
Varsome	rs199472859
LitVar	rs199472859
Map	rs199472859
PheGenI	rs199472859
Biobank	rs199472859
1000 genomes	rs199472859
hgdp	rs199472859
ensembl	rs199472859
geneview	rs199472859
scholar	rs199472859
google	rs199472859
pharmgkb	rs199472859
gwascentral	rs199472859
openSNP	rs199472859
23andMe	rs199472859
SNPshot	rs199472859
SNPdbe	rs199472859
MSV3d	rs199472859
GWAS Ctlg	rs199472859

Max Magnitude

0

ClinVar
Risk	rs199472859(C;C)
Alt	rs199472859(C;C)
Reference	Rs199472859(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.150656810A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058211.3,