rs199473499

Orientation

minus

Stabilized

minus

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

Make rs199473499(G;G)

Make rs199473499(G;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150959670

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473499
dbSNP (classic)	rs199473499
ClinGen	rs199473499
ebi	rs199473499
HLI	rs199473499
Exac	rs199473499
Gnomad	rs199473499
Varsome	rs199473499
LitVar	rs199473499
Map	rs199473499
PheGenI	rs199473499
Biobank	rs199473499
1000 genomes	rs199473499
hgdp	rs199473499
ensembl	rs199473499
geneview	rs199473499
scholar	rs199473499
google	rs199473499
pharmgkb	rs199473499
gwascentral	rs199473499
openSNP	rs199473499
23andMe	rs199473499
SNPshot	rs199473499
SNPdbe	rs199473499
MSV3d	rs199473499
GWAS Ctlg	rs199473499

Max Magnitude

0

ClinVar
Risk	rs199473499(G;G)
Alt	rs199473499(G;G)
Reference	Rs199473499(T;T)
Significance	Untested
Disease	Congenital long QT syndrome Cardiovascular phenotype
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome Cardiovascular phenotype
Reversed	1
HGVS	NC_000007.13:g.150656758A>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058231.3, RCV000246450.1,