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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) 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: 4

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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.1030G>A (p.Val344Ile)	rs199798449	0.00052
NM_004999.4(MYO6):c.475G>A (p.Glu159Lys)	rs201507590	0.00026

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