{{Rsnum
|rsid=1364705
|Gene=MAL2
|Chromosome=8
|position=119212566
|Orientation=minus
|GMAF=0.2755
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=MAL2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 4.4 | 42.5 | 53.1
| HCB | 35.8 | 47.4 | 16.8
| JPT | 23.9 | 46.9 | 29.2
| YRI | 0.0 | 10.2 | 89.8
| ASW | 0.0 | 0.0 | 0.0
| CHB | 35.8 | 47.4 | 16.8
| CHD | 36.7 | 40.4 | 22.9
| GIH | 2.0 | 28.7 | 69.3
| LWK | 0.9 | 13.6 | 85.5
| MEX | 8.8 | 33.3 | 57.9
| MKK | 0.6 | 22.4 | 76.9
| TSI | 5.9 | 41.2 | 52.9
| 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=0.000009
|OR=NR
|ORtxt=NR
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1364705
|overall_frequency_n=26
|overall_frequency_d=128
|overall_frequency=0.203125
|n_genomes=19
|n_genomes_annotated=0
|n_haplomes=23
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

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