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rs2841498

From SNPedia

Orientationplus
Stabilizedplus
Make rs2841498(A;A)
Make rs2841498(A;C)
Make rs2841498(C;C)
ReferenceGRCh38 38.1/141
Chromosome9
Position85315130
is asnp
is mentioned by
dbSNPrs2841498
ebirs2841498
HLIrs2841498
Exacrs2841498
Varsomers2841498
Maprs2841498
PheGenIrs2841498
hapmaprs2841498
1000 genomesrs2841498
hgdprs2841498
ensemblrs2841498
gopubmedrs2841498
geneviewrs2841498
scholarrs2841498
googlers2841498
pharmgkbrs2841498
gwascentralrs2841498
openSNPrs2841498
23andMers2841498
23andMe allrs2841498
SNP Nexus

SNPshotrs2841498
SNPdbers2841498
MSV3drs2841498
GWAS Ctlgrs2841498
GMAF0.1331
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 20522523OA-icon.png]
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