{{Rsnum
|rsid=10074258
|Gene=EFNA5
|Chromosome=5
|position=107646859
|Orientation=plus
|GMAF=0.3728
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=EFNA5
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 40.7 | 46.0 | 13.3
| HCB | 31.9 | 52.6 | 15.6
| JPT | 38.2 | 49.1 | 12.7
| YRI | 64.6 | 31.3 | 4.1
| ASW | 64.9 | 28.1 | 7.0
| CHB | 31.9 | 52.6 | 15.6
| CHD | 22.9 | 59.6 | 17.4
| GIH | 16.0 | 54.0 | 30.0
| LWK | 56.4 | 37.3 | 6.4
| MEX | 29.8 | 43.9 | 26.3
| MKK | 46.8 | 40.4 | 12.8
| TSI | 33.3 | 51.0 | 15.7
| 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=2E-7
|OR=NR
|ORtxt=NR
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs10074258
|overall_frequency_n=49
|overall_frequency_d=126
|overall_frequency=0.388889
|n_genomes=29
|n_genomes_annotated=0
|n_haplomes=38
|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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}