{{Rsnum
|rsid=2278107
|Gene=EPHA7
|Chromosome=6
|position=93410921
|Orientation=plus
|GMAF=0.06474
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=EPHA7
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 8.0 | 92.0
| HCB | 5.1 | 19.7 | 75.2
| JPT | 1.8 | 18.6 | 79.6
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 5.3 | 94.7
| CHB | 5.1 | 19.7 | 75.2
| CHD | 2.8 | 26.9 | 70.4
| GIH | 0.0 | 16.8 | 83.2
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 12.1 | 87.9
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 4.9 | 95.1
| HapMapRevision=28
}}{{PMID Auto
|PMID=20085586
|Title=Genome-wide identification of chemosensitive single nucleotide polymorphism markers in colorectal cancers
}}

{{PMID Auto
|PMID=18853455
|Title=Whole genome survey of coding SNPs reveals a reproducible pathway determinant of Parkinson disease.
|OA=1
}}

{{GET Evidence
|gene=EPHA7
|aa_change=Ile138Val
|aa_change_short=I138V
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2278107
|overall_frequency_n=235
|overall_frequency_d=10758
|overall_frequency=0.0218442
|n_genomes=6
|n_genomes_annotated=0
|n_haplomes=8
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.005
|nblosum100=-4
|autoscore=0
|webscore=N
}}

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