Variants in gene MYO6 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 12

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HGVS	dbSNP	gnomAD frequency
NM_004999.4(MYO6):c.1025C>T (p.Ala342Val)	rs145564837	0.00128
NM_004999.4(MYO6):c.3530G>A (p.Arg1177His)	rs139664153	0.00099
NM_004999.4(MYO6):c.92T>C (p.Ile31Thr)	rs148735953	0.00093
NM_004999.4(MYO6):c.3529C>T (p.Arg1177Cys)	rs146419641	0.00069
NM_004999.4(MYO6):c.1030G>A (p.Val344Ile)	rs199798449	0.00052
NM_004999.4(MYO6):c.1546+6T>C	rs199999513	0.00052
NM_004999.4(MYO6):c.2836C>T (p.Arg946Cys)	rs141845119	0.00039
NM_004999.4(MYO6):c.475G>A (p.Glu159Lys)	rs201507590	0.00026
NM_004999.4(MYO6):c.188-3T>C	rs373199401	0.00017
NM_004999.4(MYO6):c.262-12T>G	rs368072756	0.00017
NM_004999.4(MYO6):c.2665A>G (p.Met889Val)	rs727505098	0.00014
NM_004999.4(MYO6):c.2898AGA[3] (p.Glu970del)	rs727504743

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