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rs1490157

From SNPedia

Orientationplus
Stabilizedplus
Make rs1490157(C;C)
Make rs1490157(C;T)
Make rs1490157(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position21677754
GeneZNF385D
is asnp
is mentioned by
dbSNPrs1490157
ebirs1490157
HLIrs1490157
Exacrs1490157
Varsomers1490157
Maprs1490157
PheGenIrs1490157
hapmaprs1490157
1000 genomesrs1490157
hgdprs1490157
ensemblrs1490157
gopubmedrs1490157
geneviewrs1490157
scholarrs1490157
googlers1490157
pharmgkbrs1490157
gwascentralrs1490157
openSNPrs1490157
23andMers1490157
23andMe allrs1490157
SNP Nexus

SNPshotrs1490157
SNPdbers1490157
MSV3drs1490157
GWAS Ctlgrs1490157
GMAF0.3053
Max Magnitude
? (C;C) (C;T) (T;T) 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 0.000005
Odds Ratio 1.20 [1.11-1.32]