rs794728532

Orientation

plus

Stabilized

plus

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

Make rs794728532(G;T)

Make rs794728532(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

2768874

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs794728532
dbSNP (classic)	rs794728532
ClinGen	rs794728532
ebi	rs794728532
HLI	rs794728532
Exac	rs794728532
Gnomad	rs794728532
Varsome	rs794728532
LitVar	rs794728532
Map	rs794728532
PheGenI	rs794728532
Biobank	rs794728532
1000 genomes	rs794728532
hgdp	rs794728532
ensembl	rs794728532
geneview	rs794728532
scholar	rs794728532
google	rs794728532
pharmgkb	rs794728532
gwascentral	rs794728532
openSNP	rs794728532
23andMe	rs794728532
SNPshot	rs794728532
SNPdbe	rs794728532
MSV3d	rs794728532
GWAS Ctlg	rs794728532

Max Magnitude

0

ClinVar
Risk	rs794728532(T;T)
Alt	rs794728532(T;T)
Reference	Rs794728532(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ1
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.2790104G>T
CLNSRC
CLNACC	RCV000182195.1,