rs281865066

Orientation

minus

Stabilized

minus

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

Make rs281865066(C;T)

Make rs281865066(T;T)

Reference

GRCh38 38.1/141

Chromosome

20

Position

63350533

Gene

CHRNA4

is a	snp
is	mentioned by
dbSNP	rs281865066
dbSNP (classic)	rs281865066
ClinGen	rs281865066
ebi	rs281865066
HLI	rs281865066
Exac	rs281865066
Gnomad	rs281865066
Varsome	rs281865066
LitVar	rs281865066
Map	rs281865066
PheGenI	rs281865066
Biobank	rs281865066
1000 genomes	rs281865066
hgdp	rs281865066
ensembl	rs281865066
geneview	rs281865066
scholar	rs281865066
google	rs281865066
pharmgkb	rs281865066
gwascentral	rs281865066
openSNP	rs281865066
23andMe	rs281865066
SNPshot	rs281865066
SNPdbe	rs281865066
MSV3d	rs281865066
GWAS Ctlg	rs281865066

Max Magnitude

0

ClinVar
Risk	rs281865066(T;T)
Alt	rs281865066(T;T)
Reference	Rs281865066(C;C)
Significance	Pathogenic
Disease	Epilepsy
Variation	info
Gene	CHRNA4
CLNDBN	Epilepsy, nocturnal frontal lobe, type 1
Reversed	1
HGVS	NC_000020.10:g.61981885G>A
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000033928.2,