{{Rsnum
|rsid=8115854
|Gene=C20orf132
|Chromosome=20
|position=37137934
|Orientation=plus
|GMAF=0.3095
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=MROH8
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 46.9 | 40.7 | 12.4
| HCB | 94.9 | 5.1 | 0.0
| JPT | 98.2 | 1.8 | 0.0
| YRI | 20.5 | 53.4 | 26.0
| ASW | 12.3 | 50.9 | 36.8
| CHB | 94.9 | 5.1 | 0.0
| CHD | 95.4 | 4.6 | 0.0
| GIH | 39.6 | 52.5 | 7.9
| LWK | 13.6 | 52.7 | 33.6
| MEX | 65.5 | 29.3 | 5.2
| MKK | 23.7 | 53.8 | 22.4
| TSI | 36.3 | 50.0 | 13.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19668339
|Trait=Hippocampal atrophy
|Title=Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease
|RiskAllele=
|Pval=0.000002
|OR=NR
|ORtxt=NR
|OA=1
}}

{{GET Evidence
|gene=C20ORF132
|aa_change=Ser429Pro
|aa_change_short=S429P
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs8115854
|overall_frequency_n=52
|overall_frequency_d=128
|overall_frequency=0.40625
|n_genomes=31
|n_genomes_annotated=0
|n_haplomes=41
|n_articles=0
|n_articles_annotated=0
|nblosum100=3
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}