List of variants in gene combination CBR4, PALLD reported as benign for Hereditary cancer-predisposing syndrome

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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: 3

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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.3359-4G>A	rs112116419	0.01852
NM_001166108.2(PALLD):c.3359-24CT[5]	rs536545858

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