rs764781840

Orientation

plus

Stabilized

plus

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

Make rs764781840(C;C)

Make rs764781840(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

2572086

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs764781840
dbSNP (classic)	rs764781840
ClinGen	rs764781840
ebi	rs764781840
HLI	rs764781840
Exac	rs764781840
Gnomad	rs764781840
Varsome	rs764781840
LitVar	rs764781840
Map	rs764781840
PheGenI	rs764781840
Biobank	rs764781840
1000 genomes	rs764781840
hgdp	rs764781840
ensembl	rs764781840
geneview	rs764781840
scholar	rs764781840
google	rs764781840
pharmgkb	rs764781840
gwascentral	rs764781840
openSNP	rs764781840
23andMe	rs764781840
SNPshot	rs764781840
SNPdbe	rs764781840
MSV3d	rs764781840
GWAS Ctlg	rs764781840

Max Magnitude

0

ClinVar
Risk	rs764781840(C;C) rs764781840(G;G)
Alt	rs764781840(C;C) rs764781840(G;G)
Reference	Rs764781840(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ1
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.2593316T>C
CLNSRC
CLNACC	RCV000182107.1,