MYO6 and Autosomal Dominant Nonsyndromic Hearing Loss 22: Association Evidence

At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

Provenance

2 sources

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

MYO6

1 source summary

A gene summary alongside the source descriptions it was distilled from.

Autosomal Dominant Nonsyndromic Hearing Loss 22

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

ClinVar and variant evidence

214 clinical variants

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

Population genetics

1 GWAS phenotype

Gene-associated GWAS phenotypes matching the disorder, with best SNP, score, risk-allele frequency and effect size.

Literature

7 publications

Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.

Provenance

11 references

Every source and publication cited across this dossier, as one numbered reference list.