Related gene-specific medical variations for Gene (Select 7292) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 979308	GRCh37/hg19 1q25.1(chr1:173047673-173339681)x1	TNFSF4	Copy number loss	not provided	GUncertain significance
Select item 688914	GRCh37/hg19 1q25.1(chr1:173036654-173333855)x1	TNFSF4	Copy number loss	not provided	GUncertain significance
Select item 565197	GRCh37/hg19 1q25.1(chr1:173064278-173167101)x1	TNFSF4	Copy number loss	not provided	GLikely benign

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