Related gene-specific medical variations for Gene (Select 791115) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 564163	GRCh37/hg19 15q11.2(chr15:24348989-24782134)x1	PWRN2	Copy number loss	not provided	GLikely benign
Select item 221750	GRCh38/hg38 15q11.2(chr15:24112068-24227134)x1	PWRN2	Copy number loss	Premature ovarian failure	GBenign
Select item 157332	NR_026647.1(PWRN2):n.-56949_57842del	PWRN2	Deletion	Gestational diabetes mellitus uncontrolled	Gnot provided

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