rs199472887

Orientation

minus

Stabilized

minus

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

Make rs199472887(A;A)

Make rs199472887(A;G)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150957452

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199472887
dbSNP (classic)	rs199472887
ClinGen	rs199472887
ebi	rs199472887
HLI	rs199472887
Exac	rs199472887
Gnomad	rs199472887
Varsome	rs199472887
LitVar	rs199472887
Map	rs199472887
PheGenI	rs199472887
Biobank	rs199472887
1000 genomes	rs199472887
hgdp	rs199472887
ensembl	rs199472887
geneview	rs199472887
scholar	rs199472887
google	rs199472887
pharmgkb	rs199472887
gwascentral	rs199472887
openSNP	rs199472887
23andMe	rs199472887
SNPshot	rs199472887
SNPdbe	rs199472887
MSV3d	rs199472887
GWAS Ctlg	rs199472887

Max Magnitude

0

ClinVar
Risk	rs199472887(A;A)
Alt	rs199472887(A;A)
Reference	Rs199472887(G;G)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150654540C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058280.3,