rs199473415

Orientation

minus

Stabilized

minus

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

Make rs199473415(A;A)

Make rs199473415(A;G)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150974827

Gene	KCNH2, LOC107986861

is a	snp
is	mentioned by
dbSNP	rs199473415
dbSNP (classic)	rs199473415
ClinGen	rs199473415
ebi	rs199473415
HLI	rs199473415
Exac	rs199473415
Gnomad	rs199473415
Varsome	rs199473415
LitVar	rs199473415
Map	rs199473415
PheGenI	rs199473415
Biobank	rs199473415
1000 genomes	rs199473415
hgdp	rs199473415
ensembl	rs199473415
geneview	rs199473415
scholar	rs199473415
google	rs199473415
pharmgkb	rs199473415
gwascentral	rs199473415
openSNP	rs199473415
23andMe	rs199473415
SNPshot	rs199473415
SNPdbe	rs199473415
MSV3d	rs199473415
GWAS Ctlg	rs199473415

Max Magnitude

0

ClinVar
Risk	rs199473415(A;A)
Alt	rs199473415(A;A)
Reference	Rs199473415(G;G)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150671915C>T
CLNSRC	ClinVar
CLNACC	RCV000058054.3,