rs199473664

Orientation

minus

Stabilized

minus

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

Make rs199473664(A;A)

Make rs199473664(A;G)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150974833

Gene	KCNH2, LOC107986861

is a	snp
is	mentioned by
dbSNP	rs199473664
dbSNP (classic)	rs199473664
ClinGen	rs199473664
ebi	rs199473664
HLI	rs199473664
Exac	rs199473664
Gnomad	rs199473664
Varsome	rs199473664
LitVar	rs199473664
Map	rs199473664
PheGenI	rs199473664
Biobank	rs199473664
1000 genomes	rs199473664
hgdp	rs199473664
ensembl	rs199473664
geneview	rs199473664
scholar	rs199473664
google	rs199473664
pharmgkb	rs199473664
gwascentral	rs199473664
openSNP	rs199473664
23andMe	rs199473664
SNPshot	rs199473664
SNPdbe	rs199473664
MSV3d	rs199473664
GWAS Ctlg	rs199473664

Max Magnitude

0

ClinVar
Risk	rs199473664(A;A)
Alt	rs199473664(A;A)
Reference	Rs199473664(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.150671921C>T
CLNSRC	ClinVar
CLNACC	RCV000058016.3,