C5542197[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 132802	NM_001615.4(ACTG2):c.119G>A (p.Arg40His)	ACTG2 (R40H)	Single nucleotide variant (missense variant)	Visceral myopathy 1 +3 more	GPathogenic/Likely pathogenic
Select item 132803	NM_001615.4(ACTG2):c.769C>T (p.Arg257Cys)	ACTG2 (R257C +1 more)	Single nucleotide variant (missense variant)	Visceral myopathy 1 +4 more	GPathogenic
Select item 1032761	NM_001615.4(ACTG2):c.1031G>C (p.Gly344Ala)	ACTG2 (G301A +1 more)	Single nucleotide variant (missense variant)	Visceral myopathy 1	GUncertain significance

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