"GeneDx"[submitter] AND "LOC129929037"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1318014	NM_175875.5(SIX5):c.238C>T (p.Pro80Ser)	DM1-AS, LOC107075317 +2 more (P80S)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 1318058	NM_175875.5(SIX5):c.233C>T (p.Ser78Phe)	DM1-AS, LOC107075317 +2 more (S78F)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 500193	NM_175875.5(SIX5):c.213G>T (p.Gly71=)	DM1-AS, LOC107075317 +2 more	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1317730	NM_175875.5(SIX5):c.191C>T (p.Pro64Leu)	DM1-AS, LOC107075317 +2 more (P64L)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1318265	NM_175875.5(SIX5):c.108G>A (p.Leu36=)	DM1-AS, LOC107075317 +2 more	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1317703	NM_175875.5(SIX5):c.78A>G (p.Glu26=)	DM1-AS, LOC107075317 +2 more	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

ClinVar