List of variants in gene MYO6 reported as pathogenic for Autosomal dominant nonsyndromic hearing loss 22

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_004999.4(MYO6):c.238C>T (p.Arg80Ter)	rs727504567	0.00001
NM_004999.4(MYO6):c.2545C>T (p.Arg849Ter)	rs121912561	0.00001
NM_004999.4(MYO6):c.826C>T (p.Arg276Ter)	rs727503326	0.00001
NM_004999.4(MYO6):c.1325G>A (p.Cys442Tyr)	rs121912557
NM_004999.4(MYO6):c.1452dup (p.Asn485Ter)	rs1775958137
NM_004999.4(MYO6):c.1473_1473+2delinsC	rs878853225
NM_004999.4(MYO6):c.2417-1758T>G	rs1562283089
NM_004999.4(MYO6):c.2717C>A (p.Ser906Ter)	rs1554218566
NM_004999.4(MYO6):c.2839C>T (p.Arg947Ter)	rs876657653
NM_004999.4(MYO6):c.3765del (p.Cys1256fs)	rs1582024232
NM_004999.4(MYO6):c.406C>T (p.Arg136Ter)
NM_004999.4(MYO6):c.897G>T (p.Glu299Asp)	rs1060499799

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