rs796052196

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;T)	5	Romano-Ward Long QT Syndrome
(T;T)	0	common in clinvar

Make rs796052196(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150974709

Gene	KCNH2, LOC107986861

is a	snp
is	mentioned by
dbSNP	rs796052196
dbSNP (classic)	rs796052196
ClinGen	rs796052196
ebi	rs796052196
HLI	rs796052196
Exac	rs796052196
Gnomad	rs796052196
Varsome	rs796052196
LitVar	rs796052196
Map	rs796052196
PheGenI	rs796052196
Biobank	rs796052196
1000 genomes	rs796052196
hgdp	rs796052196
ensembl	rs796052196
geneview	rs796052196
scholar	rs796052196
google	rs796052196
pharmgkb	rs796052196
gwascentral	rs796052196
openSNP	rs796052196
23andMe	rs796052196
SNPshot	rs796052196
SNPdbe	rs796052196
MSV3d	rs796052196
GWAS Ctlg	rs796052196

Max Magnitude

5

ClinVar
Risk	rs796052196(A;A)
Alt	rs796052196(A;A)
Reference	Rs796052196(T;T)
Significance	Probable-Pathogenic
Disease	Long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150671797A>T
CLNSRC
CLNACC	RCV000190216.1,