rs796052676

Orientation

minus

Stabilized

minus

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

Make rs796052676(C;T)

Make rs796052676(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

8

Position

132180246

Gene

KCNQ3

is a	snp
is	mentioned by
dbSNP	rs796052676
dbSNP (classic)	rs796052676
ClinGen	rs796052676
ebi	rs796052676
HLI	rs796052676
Exac	rs796052676
Gnomad	rs796052676
Varsome	rs796052676
LitVar	rs796052676
Map	rs796052676
PheGenI	rs796052676
Biobank	rs796052676
1000 genomes	rs796052676
hgdp	rs796052676
ensembl	rs796052676
geneview	rs796052676
scholar	rs796052676
google	rs796052676
pharmgkb	rs796052676
gwascentral	rs796052676
openSNP	rs796052676
23andMe	rs796052676
SNPshot	rs796052676
SNPdbe	rs796052676
MSV3d	rs796052676
GWAS Ctlg	rs796052676

Max Magnitude

0

ClinVar
Risk	rs796052676(T;T)
Alt	rs796052676(T;T)
Reference	Rs796052676(C;C)
Significance	Pathogenic
Disease	not provided Benign familial neonatal seizures 2
Variation	info
Gene	KCNQ3
CLNDBN	not provided Benign familial neonatal seizures 2
Reversed	1
HGVS	NC_000008.10:g.133192493G>A
CLNSRC
CLNACC	RCV000187968.2, RCV000210407.1,