Variants in gene combination ACTC1, GJD2-DT with conflicting interpretations reported as "likely pathogenic and "uncertain significance"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_005159.5(ACTC1):c.28C>A (p.Leu10Met)	rs397517057	0.00003
NM_005159.5(ACTC1):c.310C>T (p.Pro104Ser)	rs397517059
NM_005159.5(ACTC1):c.383C>T (p.Thr128Ile)	rs727504308
NM_005159.5(ACTC1):c.554G>A (p.Arg185Gln)	rs866147243
NM_005159.5(ACTC1):c.664G>A (p.Ala222Thr)	rs1555418793
NM_005159.5(ACTC1):c.793C>G (p.Gln265Glu)	rs727504323
NM_005159.5(ACTC1):c.806T>C (p.Ile269Thr)	rs397517071

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