Related gene-specific medical variations for Gene (Select 58533) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3167331	NM_152233.4(SNX6):c.-30G>T	LOC130055472, SNX6	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3167330	NM_152233.4(SNX6):c.-18C>G	LOC130055472, SNX6	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2454486	NM_152233.4(SNX6):c.-15C>T	SNX6, LOC130055472	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2213344	NM_152233.4(SNX6):c.-12C>T	LOC130055472, SNX6	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1808095	GRCh37/hg19 14q13.1(chr14:35017859-35089000)x1	SNX6	Copy number loss	not provided	GUncertain significance
Select item 685084	GRCh37/hg19 14q13.1(chr14:35017857-35089000)x1	SNX6	Copy number loss	not provided	GUncertain significance

ClinVar