Related gene-specific medical variations for Gene (Select 1038) - ClinVar - NCBI

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Links from Gene

Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3265598	NR_173139.1(LINC00632):n.909C>T	CDR1, LINC00632	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3141695	NR_190227.1(LINC00632):n.894T>G	CDR1, LINC00632	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3141694	NR_190227.1(LINC00632):n.1084T>A	CDR1, LINC00632	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3141693	NR_190227.1(LINC00632):n.1215A>T	CDR1, LINC00632	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2661545	NR_173139.1(LINC00632):n.1482_1499del	CDR1, LINC00632	Deletion (non-coding transcript variant)	not provided	GLikely benign
Select item 2324368	NR_173139.1(LINC00632):n.1146C>G	CDR1, LINC00632	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2309179	NR_173139.1(LINC00632):n.1158T>C	CDR1, LINC00632	Single nucleotide variant (non-coding transcript variant)	not specified	GLikely benign
Select item 2300433	NR_173139.1(LINC00632):n.1212G>T	CDR1, LINC00632	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2275232	NR_173139.1(LINC00632):n.1227C>A	CDR1, LINC00632	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 789465	NM_004065.2(CDR1):c.670C>T (p.Arg224Cys)	CDR1, LINC00632	Single nucleotide variant	not provided	GBenign