rs794728527

Orientation

plus

Stabilized

plus

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

Make rs794728527(A;A)

Make rs794728527(A;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

2588844

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs794728527
dbSNP (classic)	rs794728527
ClinGen	rs794728527
ebi	rs794728527
HLI	rs794728527
Exac	rs794728527
Gnomad	rs794728527
Varsome	rs794728527
LitVar	rs794728527
Map	rs794728527
PheGenI	rs794728527
Biobank	rs794728527
1000 genomes	rs794728527
hgdp	rs794728527
ensembl	rs794728527
geneview	rs794728527
scholar	rs794728527
google	rs794728527
pharmgkb	rs794728527
gwascentral	rs794728527
openSNP	rs794728527
23andMe	rs794728527
SNPshot	rs794728527
SNPdbe	rs794728527
MSV3d	rs794728527
GWAS Ctlg	rs794728527

Max Magnitude

0

ClinVar
Risk	rs794728527(A;A) rs794728527(C;C)
Alt	rs794728527(A;A) rs794728527(C;C)
Reference	Rs794728527(T;T)
Significance	Probable-Pathogenic
Disease	not provided not specified
Variation	info
Gene	KCNQ1
CLNDBN	not provided not specified
Reversed	0
HGVS	NC_000011.9:g.2610074T>A; NC_000011.9:g.2610074T>C
CLNSRC
CLNACC	RCV000182178.1, RCV000417865.1,