Related gene-specific medical variations for Gene (Select 65975) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3338166	E446*	STK33	Single nucleotide variant	not provided	GUncertain significance
Select item 2685397	GRCh37/hg19 11p15.4(chr11:8369292-8458749)x1	STK33	Copy number loss	not provided	GUncertain significance
Select item 376702	NM_001352389.2(STK33):c.969T>G (p.Phe323Leu)	STK33 (F136L +2 more)	Single nucleotide variant (missense variant)	Neoplasm of the pancreas	GLikely pathogenic

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