rs199473506

Orientation

minus

Stabilized

minus

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

Make rs199473506(A;G)

Make rs199473506(G;G)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150952777

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473506
dbSNP (classic)	rs199473506
ClinGen	rs199473506
ebi	rs199473506
HLI	rs199473506
Exac	rs199473506
Gnomad	rs199473506
Varsome	rs199473506
LitVar	rs199473506
Map	rs199473506
PheGenI	rs199473506
Biobank	rs199473506
1000 genomes	rs199473506
hgdp	rs199473506
ensembl	rs199473506
geneview	rs199473506
scholar	rs199473506
google	rs199473506
pharmgkb	rs199473506
gwascentral	rs199473506
openSNP	rs199473506
23andMe	rs199473506
SNPshot	rs199473506
SNPdbe	rs199473506
MSV3d	rs199473506
GWAS Ctlg	rs199473506

Max Magnitude

0

ClinVar
Risk	rs199473506(G;G)
Alt	rs199473506(G;G)
Reference	Rs199473506(A;A)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150649865T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000057873.3,