rs199473026

Orientation

minus

Stabilized

minus

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

Make rs199473026(C;C)

Make rs199473026(C;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150947334

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473026
dbSNP (classic)	rs199473026
ClinGen	rs199473026
ebi	rs199473026
HLI	rs199473026
Exac	rs199473026
Gnomad	rs199473026
Varsome	rs199473026
LitVar	rs199473026
Map	rs199473026
PheGenI	rs199473026
Biobank	rs199473026
1000 genomes	rs199473026
hgdp	rs199473026
ensembl	rs199473026
geneview	rs199473026
scholar	rs199473026
google	rs199473026
pharmgkb	rs199473026
gwascentral	rs199473026
openSNP	rs199473026
23andMe	rs199473026
SNPshot	rs199473026
SNPdbe	rs199473026
MSV3d	rs199473026
GWAS Ctlg	rs199473026

Max Magnitude

0

ClinVar
Risk	rs199473026(C;C)
Alt	rs199473026(C;C)
Reference	Rs199473026(T;T)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150644422A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058203.3,