Related gene-specific medical variations for Gene (Select 29) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 768813	NM_001322841.2(ABR):c.92C>A (p.Ala31Glu)	ABR, LOC130059874 (A31E)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 689291	GRCh37/hg19 17p13.3(chr17:1002845-1139698)x3	ABR	Copy number gain	not provided	GUncertain significance
Select item 395099	GRCh37/hg19 17p13.3(chr17:961016-1077839)x1	ABR	Copy number loss	See cases	GLikely benign
Select item 151085	GRCh38/hg38 17p13.3(chr17:1078810-1170736)x1	ABR	Copy number loss	See cases	GUncertain significance

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