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

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 25

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HGVS	dbSNP	gnomAD frequency
NM_004999.4(MYO6):c.*3288T>C	rs118121148	0.00504
NM_004999.4(MYO6):c.1224-4A>G	rs144031818	0.00238
NM_004999.4(MYO6):c.*4095G>A	rs185154265	0.00152
NM_004999.4(MYO6):c.1144G>A (p.Asp382Asn)	rs111530469	0.00137
NM_004999.4(MYO6):c.2517T>C (p.Gly839=)	rs112597191	0.00137
NM_004999.4(MYO6):c.*303A>G	rs146133231	0.00128
NM_004999.4(MYO6):c.1025C>T (p.Ala342Val)	rs145564837	0.00128
NM_004999.4(MYO6):c.*1232C>T	rs182487428	0.00051
NM_004999.4(MYO6):c.2836C>T (p.Arg946Cys)	rs141845119	0.00039
NM_004999.4(MYO6):c.*3230T>C	rs562815854	0.00038
NM_004999.4(MYO6):c.*3874G>A	rs187631847	0.00032
NM_004999.4(MYO6):c.*4288G>A	rs570588843	0.00029
NM_004999.4(MYO6):c.*1738A>G	rs193019967	0.00028
NM_004999.4(MYO6):c.475G>A (p.Glu159Lys)	rs201507590	0.00025
NM_004999.4(MYO6):c.*4428A>G	rs574549669	0.00024
NM_004999.4(MYO6):c.3483G>A (p.Glu1161=)	rs139174622	0.00024
NM_004999.4(MYO6):c.3176G>C (p.Arg1059Thr)	rs202214380	0.00020
NM_004999.4(MYO6):c.*3039A>G	rs540365866	0.00019
NM_004999.4(MYO6):c.*1889A>G	rs189155544	0.00018
NM_004999.4(MYO6):c.553+10A>G	rs188959117	0.00007
NM_004999.4(MYO6):c.1180G>A (p.Val394Ile)	rs373519764	0.00006
NM_004999.4(MYO6):c.2672C>T (p.Thr891Met)	rs146682372	0.00006
NM_004999.4(MYO6):c.189T>G (p.Cys63Trp)	rs768643110	0.00002
NM_004999.4(MYO6):c.*1528C>T	rs188719640
NM_004999.4(MYO6):c.*186A>G	rs571307356

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