rs2841498

Orientation

plus

Stabilized

plus

Make rs2841498(A;A)

Make rs2841498(A;C)

Make rs2841498(C;C)

Reference

GRCh38 38.1/141

Chromosome

9

Position

85315130

is a	snp
is	mentioned by
dbSNP	rs2841498
dbSNP (classic)	rs2841498
ClinGen	rs2841498
ebi	rs2841498
HLI	rs2841498
Exac	rs2841498
Gnomad	rs2841498
Varsome	rs2841498
LitVar	rs2841498
Map	rs2841498
PheGenI	rs2841498
Biobank	rs2841498
1000 genomes	rs2841498
hgdp	rs2841498
ensembl	rs2841498
geneview	rs2841498
scholar	rs2841498
google	rs2841498
pharmgkb	rs2841498
gwascentral	rs2841498
openSNP	rs2841498
23andMe	rs2841498
SNPshot	rs2841498
SNPdbe	rs2841498
MSV3d	rs2841498
GWAS Ctlg	rs2841498

GMAF

0.1331

Max Magnitude

0

?	(A;A) (A;C) (C;C)	28

GWAS snp
PMID	[PMID 20522523]
Trait	Partial epilepsies
Title	Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study
Risk Allele
P-val	0.000004
Odds Ratio	None None