"LINC-PINT-related condition"[Disease/phenotype] AND "PreventionGeneti - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3032636	NR_109851.1(LINC-PINT):n.3215C>A	LINC-PINT	Single nucleotide variant (non-coding transcript variant)	LINC-PINT-related condition	GLikely benign
Select item 3036139	NR_109851.1(LINC-PINT):n.1409G>T	LINC-PINT	Single nucleotide variant (non-coding transcript variant)	LINC-PINT-related condition	GLikely benign
Select item 3059288	NR_109851.1(LINC-PINT):n.1396-18120C>T	LINC-PINT	Single nucleotide variant (non-coding transcript variant +1 more)	LINC-PINT-related condition	GBenign
Select item 3059947	NR_109851.1(LINC-PINT):n.1264+826C>T	LINC-PINT	Single nucleotide variant (non-coding transcript variant +1 more)	LINC-PINT-related condition	GBenign
Select item 3052262	NR_109851.1(LINC-PINT):n.920T>G	LINC-PINT	Single nucleotide variant (non-coding transcript variant)	LINC-PINT-related condition	GLikely benign

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