rs199472866

Orientation

minus

Stabilized

minus

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

Make rs199472866(A;A)

Make rs199472866(A;G)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150958484

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199472866
dbSNP (classic)	rs199472866
ClinGen	rs199472866
ebi	rs199472866
HLI	rs199472866
Exac	rs199472866
Gnomad	rs199472866
Varsome	rs199472866
LitVar	rs199472866
Map	rs199472866
PheGenI	rs199472866
Biobank	rs199472866
1000 genomes	rs199472866
hgdp	rs199472866
ensembl	rs199472866
geneview	rs199472866
scholar	rs199472866
google	rs199472866
pharmgkb	rs199472866
gwascentral	rs199472866
openSNP	rs199472866
23andMe	rs199472866
SNPshot	rs199472866
SNPdbe	rs199472866
MSV3d	rs199472866
GWAS Ctlg	rs199472866

Max Magnitude

0

ClinVar
Risk	rs199472866(A;A)
Alt	rs199472866(A;A)
Reference	Rs199472866(G;G)
Significance	Untested
Disease	Congenital long QT syndrome Long QT syndrome 2 Long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome Long QT syndrome 2 Long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150655572C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058237.3, RCV000202703.1, RCV000473244.1,