rs199473528

Orientation

minus

Stabilized

minus

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

Make rs199473528(A;G)

Make rs199473528(G;G)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150951481

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473528
dbSNP (classic)	rs199473528
ClinGen	rs199473528
ebi	rs199473528
HLI	rs199473528
Exac	rs199473528
Gnomad	rs199473528
Varsome	rs199473528
LitVar	rs199473528
Map	rs199473528
PheGenI	rs199473528
Biobank	rs199473528
1000 genomes	rs199473528
hgdp	rs199473528
ensembl	rs199473528
geneview	rs199473528
scholar	rs199473528
google	rs199473528
pharmgkb	rs199473528
gwascentral	rs199473528
openSNP	rs199473528
23andMe	rs199473528
SNPshot	rs199473528
SNPdbe	rs199473528
MSV3d	rs199473528
GWAS Ctlg	rs199473528

Max Magnitude

0

ClinVar
Risk	rs199473528(G;G)
Alt	rs199473528(G;G)
Reference	Rs199473528(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.150648569T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058051.3,