rs199473546

Orientation

minus

Stabilized

minus

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

Make rs199473546(A;G)

Make rs199473546(G;G)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150945502

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473546
dbSNP (classic)	rs199473546
ClinGen	rs199473546
ebi	rs199473546
HLI	rs199473546
Exac	rs199473546
Gnomad	rs199473546
Varsome	rs199473546
LitVar	rs199473546
Map	rs199473546
PheGenI	rs199473546
Biobank	rs199473546
1000 genomes	rs199473546
hgdp	rs199473546
ensembl	rs199473546
geneview	rs199473546
scholar	rs199473546
google	rs199473546
pharmgkb	rs199473546
gwascentral	rs199473546
openSNP	rs199473546
23andMe	rs199473546
SNPshot	rs199473546
SNPdbe	rs199473546
MSV3d	rs199473546
GWAS Ctlg	rs199473546

Max Magnitude

0

ClinVar
Risk	rs199473546(G;G)
Alt	rs199473546(G;G)
Reference	Rs199473546(A;A)
Significance	Untested
Disease	Congenital long QT syndrome not specified
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome not specified
Reversed	1
HGVS	NC_000007.13:g.150642590T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058219.3, RCV000181916.1,