Related gene-specific medical variations for Gene (Select 26100) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2671680	NM_015610.4(WIPI2):c.74+2T>G	LOC129997872, WIPI2	Single nucleotide variant (splice donor variant)	Intellectual developmental disorder with short stature and variable skeletal anomalies	GUncertain significance
Select item 1527334	GRCh37/hg19 7p22.1(chr7:5122619-5284485)	WIPI2	Copy number loss	not specified	GUncertain significance
Select item 980263	GRCh37/hg19 7p22.1(chr7:5132817-5284485)x1	WIPI2	Copy number loss	not provided	GUncertain significance

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