{{Rsnum
|rsid=2282032
|Gene=C14orf102
|Chromosome=14
|position=90292547
|Orientation=plus
|GMAF=0.1387
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=NRDE2
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 66.4 | 28.3 | 5.3
| HCB | 75.9 | 22.6 | 1.5
| JPT | 82.3 | 17.7 | 0.0
| YRI | 76.2 | 22.4 | 1.4
| ASW | 71.9 | 26.3 | 1.8
| CHB | 75.9 | 22.6 | 1.5
| CHD | 85.3 | 14.7 | 0.0
| GIH | 66.0 | 29.0 | 5.0
| LWK | 80.9 | 16.4 | 2.7
| MEX | 56.9 | 37.9 | 5.2
| MKK | 81.4 | 16.7 | 1.9
| TSI | 71.6 | 24.5 | 3.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20834067
|Trait=None
|Title=Joint influence of small-effect genetic variants on human longevity.
|RiskAllele=
|Pval=0.000001
|OR=None
|ORtxt=None
|OA=1
}}

{{PMID|11022011|OA=1
}} A second-generation genomewide screen for asthma-susceptibility alleles in a founder population.

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}
{{on chip | NatGeo2}}