rs281865070

Orientation

plus

Stabilized

plus

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

Make rs281865070(C;C)

Make rs281865070(C;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

154571746

Gene

CHRNB2

is a	snp
is	mentioned by
dbSNP	rs281865070
dbSNP (classic)	rs281865070
ClinGen	rs281865070
ebi	rs281865070
HLI	rs281865070
Exac	rs281865070
Gnomad	rs281865070
Varsome	rs281865070
LitVar	rs281865070
Map	rs281865070
PheGenI	rs281865070
Biobank	rs281865070
1000 genomes	rs281865070
hgdp	rs281865070
ensembl	rs281865070
geneview	rs281865070
scholar	rs281865070
google	rs281865070
pharmgkb	rs281865070
gwascentral	rs281865070
openSNP	rs281865070
23andMe	rs281865070
SNPshot	rs281865070
SNPdbe	rs281865070
MSV3d	rs281865070
GWAS Ctlg	rs281865070

Max Magnitude

0

ClinVar
Risk	rs281865070(C;C)
Alt	rs281865070(C;C)
Reference	Rs281865070(T;T)
Significance	Pathogenic
Disease	Epilepsy not provided
Variation	info
Gene	CHRNB2
CLNDBN	Epilepsy, nocturnal frontal lobe, type 3 not provided
Reversed	0
HGVS	NC_000001.10:g.154544222T>C
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000033932.2, RCV000430538.1,