rs199472898

Orientation

minus

Stabilized

minus

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

Make rs199472898(C;C)

Make rs199472898(C;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150952703

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199472898
dbSNP (classic)	rs199472898
ClinGen	rs199472898
ebi	rs199472898
HLI	rs199472898
Exac	rs199472898
Gnomad	rs199472898
Varsome	rs199472898
LitVar	rs199472898
Map	rs199472898
PheGenI	rs199472898
Biobank	rs199472898
1000 genomes	rs199472898
hgdp	rs199472898
ensembl	rs199472898
geneview	rs199472898
scholar	rs199472898
google	rs199472898
pharmgkb	rs199472898
gwascentral	rs199472898
openSNP	rs199472898
23andMe	rs199472898
SNPshot	rs199472898
SNPdbe	rs199472898
MSV3d	rs199472898
GWAS Ctlg	rs199472898

Max Magnitude

0

ClinVar
Risk	rs199472898(C;C)
Alt	rs199472898(C;C)
Reference	Rs199472898(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.150649791A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000057883.3,