rs281865072

Orientation

plus

Stabilized

plus

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

Make rs281865072(G;G)

Make rs281865072(G;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

154571833

Gene

CHRNB2

is a	snp
is	mentioned by
dbSNP	rs281865072
dbSNP (classic)	rs281865072
ClinGen	rs281865072
ebi	rs281865072
HLI	rs281865072
Exac	rs281865072
Gnomad	rs281865072
Varsome	rs281865072
LitVar	rs281865072
Map	rs281865072
PheGenI	rs281865072
Biobank	rs281865072
1000 genomes	rs281865072
hgdp	rs281865072
ensembl	rs281865072
geneview	rs281865072
scholar	rs281865072
google	rs281865072
pharmgkb	rs281865072
gwascentral	rs281865072
openSNP	rs281865072
23andMe	rs281865072
SNPshot	rs281865072
SNPdbe	rs281865072
MSV3d	rs281865072
GWAS Ctlg	rs281865072

Max Magnitude

0

ClinVar
Risk	rs281865072(A;A) rs281865072(G;G)
Alt	rs281865072(A;A) rs281865072(G;G)
Reference	Rs281865072(T;T)
Significance	Pathogenic
Disease	Epilepsy
Variation	info
Gene	CHRNB2
CLNDBN	Epilepsy, nocturnal frontal lobe, type 3
Reversed	0
HGVS	NC_000001.10:g.154544309T>G
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000033929.2,