rs199473509

Orientation

minus

Stabilized

minus

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

Make rs199473509(C;T)

Make rs199473509(T;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150952663

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473509
dbSNP (classic)	rs199473509
ClinGen	rs199473509
ebi	rs199473509
HLI	rs199473509
Exac	rs199473509
Gnomad	rs199473509
Varsome	rs199473509
LitVar	rs199473509
Map	rs199473509
PheGenI	rs199473509
Biobank	rs199473509
1000 genomes	rs199473509
hgdp	rs199473509
ensembl	rs199473509
geneview	rs199473509
scholar	rs199473509
google	rs199473509
pharmgkb	rs199473509
gwascentral	rs199473509
openSNP	rs199473509
23andMe	rs199473509
SNPshot	rs199473509
SNPdbe	rs199473509
MSV3d	rs199473509
GWAS Ctlg	rs199473509

Max Magnitude

0

ClinVar
Risk	rs199473509(T;T)
Alt	rs199473509(T;T)
Reference	Rs199473509(C;C)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150649751G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000057892.3,