{{Rsnum
|rsid=1490157
|Gene=ZNF385D
|Chromosome=3
|position=21677754
|Orientation=plus
|GMAF=0.3053
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=ZNF385D
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 7.1 | 33.6 | 59.3
| HCB | 14.8 | 43.7 | 41.5
| JPT | 5.4 | 55.0 | 39.6
| YRI | 14.6 | 44.4 | 41.0
| ASW | 15.8 | 52.6 | 31.6
| CHB | 14.8 | 43.7 | 41.5
| CHD | 13.9 | 40.7 | 45.4
| GIH | 6.0 | 39.0 | 55.0
| LWK | 24.8 | 44.0 | 31.2
| MEX | 8.8 | 24.6 | 66.7
| MKK | 9.0 | 41.9 | 49.0
| TSI | 5.0 | 35.0 | 60.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20522523
|Trait=Partial epilepsies
|Title=Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study
|RiskAllele=
|Pval=0.000005
|OR=1.20
|ORtxt=[1.11-1.32]
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}