Related gene-specific medical variations for Gene (Select 65057) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1319341	NM_001082486.2(ACD):c.337-6C>T	ACD	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1147230	NM_001013838.3(CARMIL2):c.4305C>T (p.Pro1435=)	ACD, CARMIL2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign