"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "STK25"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2652114	NM_014808.4(FARP2):c.3159G>A (p.Glu1053=)	FARP2, STK25	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
Select item 1711534	GRCh37/hg19 2q37.3(chr2:239229304-243199373)x1	CAPN10, COPS9 +39 more	Copy number loss	not provided	GPathogenic
Select item 809210	GRCh37/hg19 2q37.3(chr2:241404033-242684292)x1	ANO7, AQP12A +24 more	Copy number loss	not provided	GUncertain significance

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