"Ambry Genetics"[submitter] AND "LOC130055992"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3184402	NM_015351.2(TTC9):c.284G>C (p.Gly95Ala)	LOC130055992, TTC9 (G95A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184403	NM_015351.2(TTC9):c.308C>T (p.Pro103Leu)	LOC130055992, TTC9 (P103L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353456	NM_015351.2(TTC9):c.329T>C (p.Leu110Pro)	LOC130055992, TTC9 (L110P)	Single nucleotide variant (missense variant)	not specified	GLikely benign

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