rs794728573

Orientation

plus

Stabilized

plus

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

Make rs794728573(A;G)

Make rs794728573(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

2768842

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs794728573
dbSNP (classic)	rs794728573
ClinGen	rs794728573
ebi	rs794728573
HLI	rs794728573
Exac	rs794728573
Gnomad	rs794728573
Varsome	rs794728573
LitVar	rs794728573
Map	rs794728573
PheGenI	rs794728573
Biobank	rs794728573
1000 genomes	rs794728573
hgdp	rs794728573
ensembl	rs794728573
geneview	rs794728573
scholar	rs794728573
google	rs794728573
pharmgkb	rs794728573
gwascentral	rs794728573
openSNP	rs794728573
23andMe	rs794728573
SNPshot	rs794728573
SNPdbe	rs794728573
MSV3d	rs794728573
GWAS Ctlg	rs794728573

Max Magnitude

0

ClinVar
Risk	rs794728573(G;G)
Alt	rs794728573(G;G)
Reference	Rs794728573(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ1
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.2790072A>G
CLNSRC
CLNACC	RCV000182319.1,