rs794728526

Orientation

plus

Stabilized

plus

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

Make rs794728526(A;T)

Make rs794728526(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

2585302

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs794728526
dbSNP (classic)	rs794728526
ClinGen	rs794728526
ebi	rs794728526
HLI	rs794728526
Exac	rs794728526
Gnomad	rs794728526
Varsome	rs794728526
LitVar	rs794728526
Map	rs794728526
PheGenI	rs794728526
Biobank	rs794728526
1000 genomes	rs794728526
hgdp	rs794728526
ensembl	rs794728526
geneview	rs794728526
scholar	rs794728526
google	rs794728526
pharmgkb	rs794728526
gwascentral	rs794728526
openSNP	rs794728526
23andMe	rs794728526
SNPshot	rs794728526
SNPdbe	rs794728526
MSV3d	rs794728526
GWAS Ctlg	rs794728526

Max Magnitude

0

ClinVar
Risk	rs794728526(G;G) rs794728526(T;T)
Alt	rs794728526(G;G) rs794728526(T;T)
Reference	Rs794728526(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ1
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.2606532A>T
CLNSRC
CLNACC	RCV000182176.2,