"Ambry Genetics"[submitter] AND "LOC129994296"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2211589	NM_180991.5(SLCO4C1):c.115C>A (p.Pro39Thr)	LOC129994296, SLCO4C1 (P39T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2323181	NM_180991.5(SLCO4C1):c.56T>G (p.Ile19Ser)	LOC129994296, SLCO4C1 (I19S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278540	NM_180991.5(SLCO4C1):c.50C>T (p.Pro17Leu)	LOC129994296, SLCO4C1 (P17L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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ClinVar