Related gene-specific medical variations for Gene (Select 92017) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1808469	GRCh37/hg19 16p13.13(chr16:12170523-12374728)x3	SNX29	Copy number gain	not provided	GUncertain significance
Select item 1340789	GRCh37/hg19 16p13.13(chr16:12278972-12338544)x1	SNX29	Copy number loss	not provided	GLikely benign
Select item 994097	NM_032167.5(SNX29):c.1363_1364del (p.Leu455fs)	SNX29 (L455fs)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 980086	GRCh37/hg19 16p13.13(chr16:12117856-12374728)x3	SNX29	Copy number gain	not provided	GUncertain significance
Select item 980084	GRCh37/hg19 16p13.13(chr16:12204015-12420150)x1	SNX29	Copy number loss	not provided	GLikely benign
Select item 564276	GRCh37/hg19 16p13.13(chr16:12327596-12397665)x1	SNX29	Copy number loss	not provided	GLikely benign
Select item 564275	GRCh37/hg19 16p13.13(chr16:12120389-12452622)x1	SNX29	Copy number loss	not provided	GLikely benign
Select item 394836	GRCh37/hg19 16p13.13-13.12(chr16:12239818-12652287)x3	SNX29	Copy number gain	See cases	GLikely benign

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