rs10496964

Orientation

plus

Stabilized

plus

Make rs10496964(C;C)

Make rs10496964(C;T)

Make rs10496964(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

144602342

is a	snp
is	mentioned by
dbSNP	rs10496964
dbSNP (classic)	rs10496964
ClinGen	rs10496964
ebi	rs10496964
HLI	rs10496964
Exac	rs10496964
Gnomad	rs10496964
Varsome	rs10496964
LitVar	rs10496964
Map	rs10496964
PheGenI	rs10496964
Biobank	rs10496964
1000 genomes	rs10496964
hgdp	rs10496964
ensembl	rs10496964
geneview	rs10496964
scholar	rs10496964
google	rs10496964
pharmgkb	rs10496964
gwascentral	rs10496964
openSNP	rs10496964
23andMe	rs10496964
SNPshot	rs10496964
SNPdbe	rs10496964
MSV3d	rs10496964
GWAS Ctlg	rs10496964

GMAF

0.124

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 22949513]
Trait	Epilepsy (generalized)
Title	Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32
Risk Allele	C
P-val	9E-9
Odds Ratio	1.47 [1.28-1.67]