{{Rsnum
|rsid=754554
|Gene=DFNA5
|Chromosome=7
|position=24719199
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=A
|GMAF=0.242
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=DFNA5
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 3.5 | 24.8 | 71.7
| HCB | 28.6 | 45.1 | 26.3
| JPT | 19.6 | 50.0 | 30.4
| YRI | 4.8 | 29.0 | 66.2
| ASW | 1.8 | 38.6 | 59.6
| CHB | 28.6 | 45.1 | 26.3
| CHD | 19.3 | 57.8 | 22.9
| GIH | 7.0 | 38.0 | 55.0
| LWK | 2.8 | 23.9 | 73.4
| MEX | 1.7 | 22.4 | 75.9
| MKK | 3.8 | 32.7 | 63.5
| TSI | 3.9 | 19.6 | 76.5
| HapMapRevision=28
}}{{Venter SNP
|rsid=754554
|allele=T
|frequency=0.119
|uid=1103652524659
|type=heterozygous_SNP
|hugo=DFNA5
|ensembl gene=ENSG00000105928
|ensembl transcript=ENST00000342947
|sift=TOLERATED
|disease=Defects in DFNA5 are the cause of autosomal dominant nonsyndromic sensorineural deafness type 5 (DFNA5) (MIM:600994).
}}

{{GET Evidence
|gene=DFNA5
|aa_change=Pro142Thr
|aa_change_short=P142T
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs754554
|overall_frequency_n=1791
|overall_frequency_d=10758
|overall_frequency=0.166481
|n_genomes=23
|n_genomes_annotated=0
|n_haplomes=27
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|pph2_score=0.292
|genetests_testable=Y
|nblosum100=4
|autoscore=1
|webscore=N
}}

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