rs199473439

Orientation

minus

Stabilized

minus

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

Make rs199473439(A;A)

Make rs199473439(A;G)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150947806

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473439
dbSNP (classic)	rs199473439
ClinGen	rs199473439
ebi	rs199473439
HLI	rs199473439
Exac	rs199473439
Gnomad	rs199473439
Varsome	rs199473439
LitVar	rs199473439
Map	rs199473439
PheGenI	rs199473439
Biobank	rs199473439
1000 genomes	rs199473439
hgdp	rs199473439
ensembl	rs199473439
geneview	rs199473439
scholar	rs199473439
google	rs199473439
pharmgkb	rs199473439
gwascentral	rs199473439
openSNP	rs199473439
23andMe	rs199473439
SNPshot	rs199473439
SNPdbe	rs199473439
MSV3d	rs199473439
GWAS Ctlg	rs199473439

Max Magnitude

0

ClinVar
Risk	rs199473439(A;A)
Alt	rs199473439(A;A)
Reference	Rs199473439(G;G)
Significance	Untested
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.150644894C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058162.3, RCV000471859.1,