List of variants in gene combination CBR4, PALLD reported as benign for adenocarcinoma

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_001166108.2(PALLD):c.2679A>G (p.Arg893=)	rs1059444	0.12743
NM_001166108.2(PALLD):c.3297T>C (p.Tyr1099=)	rs114593924	0.00564
NM_001166108.2(PALLD):c.2442A>G (p.Thr814=)	rs113676921	0.00218
NM_001166108.2(PALLD):c.3256C>T (p.Leu1086=)	rs59633770	0.00098
NM_001166108.2(PALLD):c.2199+8G>A	rs200060953	0.00070
NM_001166108.2(PALLD):c.2748C>T (p.Asp916=)	rs143544548	0.00039
NM_001166108.2(PALLD):c.2892T>C (p.Asp964=)	rs140584890	0.00028
NM_001166108.2(PALLD):c.2472+13A>G	rs190608408	0.00018
NM_001166108.2(PALLD):c.2784T>C (p.Pro928=)	rs114250766	0.00010
NM_001166108.2(PALLD):c.2199+5del	rs376654786

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