{{Rsnum
|rsid=17567
|Gene=EPS15
|Chromosome=1
|position=51361249
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=G
|GMAF=0.2346
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=EPS15
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 5.3 | 31.9 | 62.8
| HCB | 0.0 | 5.1 | 94.9
| JPT | 0.0 | 1.8 | 98.2
| YRI | 25.9 | 57.1 | 17.0
| ASW | 36.8 | 40.4 | 22.8
| CHB | 0.0 | 5.1 | 94.9
| CHD | 0.0 | 0.0 | 0.0
| GIH | 1.0 | 14.9 | 84.2
| LWK | 41.8 | 43.6 | 14.5
| MEX | 1.7 | 20.7 | 77.6
| MKK | 20.0 | 56.8 | 23.2
| TSI | 4.9 | 46.1 | 49.0
| HapMapRevision=28
}}

{{Venter SNP
|rsid=17567
|allele=C
|frequency=0.208
|uid=1103675091307
|type=heterozygous_SNP
|hugo=EPS15
|ensembl gene=ENSG00000085832
|ensembl transcript=ENST00000262674
|sift=TOLERATED
|disease=A chromosomal aberration involving EPS15 is found in acute leukemias. Translocation t(1;11)(p32;q23) with MLL/HRX. The result is a rogue activator protein.
}}

{{PMID Auto
|PMID=15986317
|Title=Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease.
|OA=1
}}

{{PMID Auto
|PMID=19633731
|Title=Association of the single nucleotide polymorphisms in the extracellular matrix metalloprotease-9 gene with PACG in southern China.
|OA=1
}}

{{GET Evidence
|gene=EPS15
|aa_change=Ile822Met
|aa_change_short=I822M
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs17567
|overall_frequency_n=3532
|overall_frequency_d=10758
|overall_frequency=0.328314
|n_genomes=29
|n_genomes_annotated=0
|n_haplomes=38
|n_articles=0
|n_articles_annotated=0
|nblosum100=-1
|autoscore=0
|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 | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}