rs13026414

Orientation

plus

Stabilized

plus

Make rs13026414(C;C)

Make rs13026414(C;T)

Make rs13026414(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

57706920

Gene	LOC101927235, LOC105377632

is a	snp
is	mentioned by
dbSNP	rs13026414
dbSNP (classic)	rs13026414
ClinGen	rs13026414
ebi	rs13026414
HLI	rs13026414
Exac	rs13026414
Gnomad	rs13026414
Varsome	rs13026414
LitVar	rs13026414
Map	rs13026414
PheGenI	rs13026414
Biobank	rs13026414
1000 genomes	rs13026414
hgdp	rs13026414
ensembl	rs13026414
geneview	rs13026414
scholar	rs13026414
google	rs13026414
pharmgkb	rs13026414
gwascentral	rs13026414
openSNP	rs13026414
23andMe	rs13026414
SNPshot	rs13026414
SNPdbe	rs13026414
MSV3d	rs13026414
GWAS Ctlg	rs13026414

GMAF

0.2612

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	2E-9
Odds Ratio	1.23 [1.15-1.32]