rs118192251

Orientation

minus

Stabilized

minus

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

Make rs118192251(C;T)

Make rs118192251(T;T)

Reference

GRCh38 38.1/141

Chromosome

8

Position

132174295

Gene

KCNQ3

is a	snp
is	mentioned by
dbSNP	rs118192251
dbSNP (classic)	rs118192251
ClinGen	rs118192251
ebi	rs118192251
HLI	rs118192251
Exac	rs118192251
Gnomad	rs118192251
Varsome	rs118192251
LitVar	rs118192251
Map	rs118192251
PheGenI	rs118192251
Biobank	rs118192251
1000 genomes	rs118192251
hgdp	rs118192251
ensembl	rs118192251
geneview	rs118192251
scholar	rs118192251
google	rs118192251
pharmgkb	rs118192251
gwascentral	rs118192251
openSNP	rs118192251
23andMe	rs118192251
SNPshot	rs118192251
SNPdbe	rs118192251
MSV3d	rs118192251
GWAS Ctlg	rs118192251

Max Magnitude

0

ClinVar
Risk	rs118192251(T;T)
Alt	rs118192251(T;T)
Reference	Rs118192251(C;C)
Significance	Pathogenic
Disease	Benign familial neonatal seizures 2 Benign familial neonatal seizures
Variation	info
Gene	KCNQ3
CLNDBN	Benign familial neonatal seizures 2 Benign familial neonatal seizures
Reversed	1
HGVS	NC_000008.10:g.133186542G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000020602.2, RCV000462450.1,