rs794728467

Orientation

minus

Stabilized

minus

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

Make rs794728467(-;GCGG)

Make rs794728467(GCGG;GCGG)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150947380

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728467
dbSNP (classic)	rs794728467
ClinGen	rs794728467
ebi	rs794728467
HLI	rs794728467
Exac	rs794728467
Gnomad	rs794728467
Varsome	rs794728467
LitVar	rs794728467
Map	rs794728467
PheGenI	rs794728467
Biobank	rs794728467
1000 genomes	rs794728467
hgdp	rs794728467
ensembl	rs794728467
geneview	rs794728467
scholar	rs794728467
google	rs794728467
pharmgkb	rs794728467
gwascentral	rs794728467
openSNP	rs794728467
23andMe	rs794728467
SNPshot	rs794728467
SNPdbe	rs794728467
MSV3d	rs794728467
GWAS Ctlg	rs794728467

Max Magnitude

0

ClinVar
Risk	rs794728467(GGCGG;GGCGG) rs794728467(GCGG;GCGG)
Alt	rs794728467(GGCGG;GGCGG) rs794728467(GCGG;GCGG)
Reference	Rs794728467(-;-)
Significance	Pathogenic
Disease	Cardiac arrhythmia not provided
Variation	info
Gene	KCNH2
CLNDBN	Cardiac arrhythmia not provided
Reversed	1
HGVS	NC_000007.13:g.150644469_150644472dupCCGC; NC_000007.13:g.150644469_150644473dupCCGCC
CLNSRC
CLNACC	RCV000182007.1, RCV000223868.1,