"PreventionGenetics, part of Exact Sciences"[submitter] AND "SPINK2"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3055956	NM_001271718.2(SPINK2):c.*153dup	SPINK2	Duplication (3 prime UTR variant +2 more)	SPINK2-related condition	GBenign
Select item 3053347	NM_001271718.2(SPINK2):c.216C>T (p.Ile72=)	SPINK2	Single nucleotide variant (synonymous variant +2 more)	SPINK2-related condition	GBenign
Select item 3042631	NM_001271718.2(SPINK2):c.205+7del	SPINK2	Deletion (non-coding transcript variant +1 more)	SPINK2-related condition	GLikely benign
Select item 3058909	NM_001271718.2(SPINK2):c.118A>G (p.Thr40Ala)	LOC129992634, SPINK2 (T40A)	Single nucleotide variant (missense variant +2 more)	SPINK2-related condition	GBenign
Select item 3059829	NM_001271718.2(SPINK2):c.110G>A (p.Gly37Glu)	LOC129992634, SPINK2 (G37E)	Single nucleotide variant (missense variant +2 more)	SPINK2-related condition	GBenign
Select item 3034488	NM_001271718.2(SPINK2):c.-7G>C	LOC129992634, SPINK2	Single nucleotide variant (5 prime UTR variant +1 more)	SPINK2-related condition	GLikely benign

ClinVar