rs199473547

Orientation

minus

Stabilized

minus

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

Make rs199473547(A;A)

Make rs199473547(A;G)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150945441

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473547
dbSNP (classic)	rs199473547
ClinGen	rs199473547
ebi	rs199473547
HLI	rs199473547
Exac	rs199473547
Gnomad	rs199473547
Varsome	rs199473547
LitVar	rs199473547
Map	rs199473547
PheGenI	rs199473547
Biobank	rs199473547
1000 genomes	rs199473547
hgdp	rs199473547
ensembl	rs199473547
geneview	rs199473547
scholar	rs199473547
google	rs199473547
pharmgkb	rs199473547
gwascentral	rs199473547
openSNP	rs199473547
23andMe	rs199473547
SNPshot	rs199473547
SNPdbe	rs199473547
MSV3d	rs199473547
GWAS Ctlg	rs199473547

Max Magnitude

0

ClinVar
Risk	rs199473547(A;A)
Alt	rs199473547(A;A)
Reference	Rs199473547(G;G)
Significance	Untested
Disease	Short QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	short QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150642529C>T
CLNSRC	ClinVar
CLNACC	RCV000058222.3,