Related gene-specific medical variations for Gene (Select 8612) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2599563	NM_003712.4(PLPP2):c.52+259C>T	PLPP2, LOC108281123 (P14L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2528290	NM_003712.4(PLPP2):c.52+246C>T	LOC108281123, PLPP2 (R10W)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 395444	GRCh37/hg19 19p13.3(chr19:277373-291274)x3	PLPP2	Copy number gain	See cases	GBenign

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