rs766616232

Orientation

plus

Stabilized

plus

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

Make rs766616232(C;T)

Make rs766616232(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

2587642

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs766616232
dbSNP (classic)	rs766616232
ClinGen	rs766616232
ebi	rs766616232
HLI	rs766616232
Exac	rs766616232
Gnomad	rs766616232
Varsome	rs766616232
LitVar	rs766616232
Map	rs766616232
PheGenI	rs766616232
Biobank	rs766616232
1000 genomes	rs766616232
hgdp	rs766616232
ensembl	rs766616232
geneview	rs766616232
scholar	rs766616232
google	rs766616232
pharmgkb	rs766616232
gwascentral	rs766616232
openSNP	rs766616232
23andMe	rs766616232
SNPshot	rs766616232
SNPdbe	rs766616232
MSV3d	rs766616232
GWAS Ctlg	rs766616232

Max Magnitude

0

ClinVar
Risk	rs766616232(T;T)
Alt	rs766616232(T;T)
Reference	Rs766616232(C;C)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	KCNQ1
CLNDBN	not specified
Reversed	0
HGVS	NC_000011.9:g.2608872C>T
CLNSRC
CLNACC	RCV000182317.2,