rs794728379

Orientation

minus

Stabilized

minus

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

Make rs794728379(A;A)

Make rs794728379(A;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150951477

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728379
dbSNP (classic)	rs794728379
ClinGen	rs794728379
ebi	rs794728379
HLI	rs794728379
Exac	rs794728379
Gnomad	rs794728379
Varsome	rs794728379
LitVar	rs794728379
Map	rs794728379
PheGenI	rs794728379
Biobank	rs794728379
1000 genomes	rs794728379
hgdp	rs794728379
ensembl	rs794728379
geneview	rs794728379
scholar	rs794728379
google	rs794728379
pharmgkb	rs794728379
gwascentral	rs794728379
openSNP	rs794728379
23andMe	rs794728379
SNPshot	rs794728379
SNPdbe	rs794728379
MSV3d	rs794728379
GWAS Ctlg	rs794728379

Max Magnitude

0

ClinVar
Risk	rs794728379(A;A)
Alt	rs794728379(A;A)
Reference	Rs794728379(T;T)
Significance	Pathogenic
Disease	Cardiac arrhythmia
Variation	info
Gene	KCNH2
CLNDBN	Cardiac arrhythmia
Reversed	1
HGVS	NC_000007.13:g.150648565A>T
CLNSRC
CLNACC	RCV000181829.1,