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rs2172802

From SNPedia

Orientationplus
Stabilizedplus
Make rs2172802(A;A)
Make rs2172802(A;G)
Make rs2172802(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position61587491
GeneLPHN3
is asnp
is mentioned by
dbSNPrs2172802
ebirs2172802
HLIrs2172802
Exacrs2172802
Varsomers2172802
Maprs2172802
PheGenIrs2172802
hapmaprs2172802
1000 genomesrs2172802
hgdprs2172802
ensemblrs2172802
gopubmedrs2172802
geneviewrs2172802
scholarrs2172802
googlers2172802
pharmgkbrs2172802
gwascentralrs2172802
openSNPrs2172802
23andMers2172802
23andMe allrs2172802
SNP Nexus

SNPshotrs2172802
SNPdbers2172802
MSV3drs2172802
GWAS Ctlgrs2172802
GMAF0.4421
Max Magnitude
? (A;A) (A;G) (G;G) 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 0.000003
Odds Ratio None None