"Ambry Genetics"[submitter] AND "LOC129992634"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2322476	NM_001271718.2(SPINK2):c.52G>A (p.Ala18Thr)	LOC129992634, SPINK2 (A18T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3322244	NM_001271718.2(SPINK2):c.29T>G (p.Leu10Arg)	LOC129992634, SPINK2 (L10R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance