rs794728516

Orientation

plus

Stabilized

plus

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

Make rs794728516(A;C)

Make rs794728516(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

2583466

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs794728516
dbSNP (classic)	rs794728516
ClinGen	rs794728516
ebi	rs794728516
HLI	rs794728516
Exac	rs794728516
Gnomad	rs794728516
Varsome	rs794728516
LitVar	rs794728516
Map	rs794728516
PheGenI	rs794728516
Biobank	rs794728516
1000 genomes	rs794728516
hgdp	rs794728516
ensembl	rs794728516
geneview	rs794728516
scholar	rs794728516
google	rs794728516
pharmgkb	rs794728516
gwascentral	rs794728516
openSNP	rs794728516
23andMe	rs794728516
SNPshot	rs794728516
SNPdbe	rs794728516
MSV3d	rs794728516
GWAS Ctlg	rs794728516

Max Magnitude

0

ClinVar
Risk	rs794728516(C;C)
Alt	rs794728516(C;C)
Reference	Rs794728516(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ1
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.2604696A>C
CLNSRC
CLNACC	RCV000182141.2,