rs199472885

Orientation

minus

Stabilized

minus

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

Make rs199472885(C;T)

Make rs199472885(T;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150957485

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199472885
dbSNP (classic)	rs199472885
ClinGen	rs199472885
ebi	rs199472885
HLI	rs199472885
Exac	rs199472885
Gnomad	rs199472885
Varsome	rs199472885
LitVar	rs199472885
Map	rs199472885
PheGenI	rs199472885
Biobank	rs199472885
1000 genomes	rs199472885
hgdp	rs199472885
ensembl	rs199472885
geneview	rs199472885
scholar	rs199472885
google	rs199472885
pharmgkb	rs199472885
gwascentral	rs199472885
openSNP	rs199472885
23andMe	rs199472885
SNPshot	rs199472885
SNPdbe	rs199472885
MSV3d	rs199472885
GWAS Ctlg	rs199472885

Max Magnitude

0

ClinVar
Risk	rs199472885(T;T)
Alt	rs199472885(T;T)
Reference	Rs199472885(C;C)
Significance	Other
Disease	Congenital long QT syndrome Long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome Long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150654573G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058276.3, RCV000171561.2,