ClinVar Miner

List of variants studied for autosomal recessive nonsyndromic hearing loss 22 by The Shared Resource Centre "Genome", Research Centre for Medical Genetics

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NC_000016.10:g.(?_21624041)_(21730798_?)del
NM_144672.4(OTOA):c.562_569dup (p.Phe191fs)

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