Variants in gene MYL3 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000258.3(MYL3):c.307+15C>T	rs184025552	0.00036
NM_000258.3(MYL3):c.4G>C (p.Ala2Pro)	rs148310342	0.00012
NM_000258.3(MYL3):c.*9C>T	rs202234617	0.00007
NM_000258.3(MYL3):c.92G>A (p.Arg31His)	rs199639940	0.00003
NM_000258.3(MYL3):c.367A>G (p.Lys123Glu)	rs536445081	0.00002
NM_000258.3(MYL3):c.532G>A (p.Asp178Asn)	rs145520567	0.00002
NM_000258.3(MYL3):c.220G>A (p.Gly74Arg)	rs730880956	0.00001
NM_000258.3(MYL3):c.560-15T>G	rs1041055773	0.00001
NM_000258.3(MYL3):c.170C>A (p.Ala57Asp)	rs139794067
NM_000258.3(MYL3):c.36T>G (p.Asp12Glu)	rs138567316

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