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rs39861

From SNPedia

Orientationminus
Stabilizedminus
Make rs39861(C;C)
Make rs39861(C;T)
Make rs39861(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position66856430
GeneMAST4
is asnp
is mentioned by
dbSNPrs39861
ebirs39861
HLIrs39861
Exacrs39861
Varsomers39861
Maprs39861
PheGenIrs39861
hapmaprs39861
1000 genomesrs39861
hgdprs39861
ensemblrs39861
gopubmedrs39861
geneviewrs39861
scholarrs39861
googlers39861
pharmgkbrs39861
gwascentralrs39861
openSNPrs39861
23andMers39861
23andMe allrs39861
SNP Nexus

SNPshotrs39861
SNPdbers39861
MSV3drs39861
GWAS Ctlgrs39861
GMAF0.2755
Max Magnitude
? (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 3E-7
Odds Ratio 1.26 [1.13-1.41]