{{Rsnum
|rsid=9493627
|Gene=EYA4
|Chromosome=6
|position=133468590
|Orientation=plus
|GMAF=0.3926
|Gene_s=EYA4,KRT8P21
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 8.0 | 48.2 | 43.8
| HCB | 20.7 | 44.4 | 34.8
| JPT | 15.0 | 39.8 | 45.1
| YRI | 33.3 | 47.6 | 19.0
| ASW | 31.6 | 43.9 | 24.6
| CHB | 20.7 | 44.4 | 34.8
| CHD | 14.8 | 40.7 | 44.4
| GIH | 24.8 | 42.6 | 32.7
| LWK | 34.5 | 50.0 | 15.5
| MEX | 15.5 | 37.9 | 46.6
| MKK | 46.8 | 42.3 | 10.9
| TSI | 8.8 | 50.0 | 41.2
| HapMapRevision=28
}}{{Venter SNP
|rsid=9493627
|allele=A
|frequency=0.302
|uid=1103705013114
|type=heterozygous_SNP
|hugo=EYA4
|ensembl gene=ENSG00000112319
|ensembl transcript=ENST00000358521
|sift=TOLERATED
|disease=Defects in EYA4 are the cause of dilated cardiomyopathy 1J (CMD1J) (MIM:605362). CMD1J is an autosomal dominant disorder characterized by sensorineural hearing loss and dilated cardiomyopathy in the absence of other anomalies.
}}

{{GET Evidence
|gene=EYA4
|aa_change=Gly277Ser
|aa_change_short=G277S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs9493627
|overall_frequency_n=4149
|overall_frequency_d=10758
|overall_frequency=0.385666
|n_genomes=34
|n_genomes_annotated=0
|n_haplomes=43
|n_articles=0
|n_articles_annotated=0
|qualityscore_in_silico=5
|qualitycomment_in_silico=Y
|gene_in_genetests=Y
|pph2_score=0.697
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=2
|autoscore=2
|webscore=N
}}

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