List of variants in gene RET reported as likely pathogenic for Hereditary cancer-predisposing syndrome

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.2410G>A (p.Val804Met)	rs79658334	0.00022
NM_020975.6(RET):c.2752A>G (p.Met918Val)	rs377767442	0.00001
NM_020975.6(RET):c.1664T>G (p.Phe555Cys)	rs2538470328
NM_020975.6(RET):c.1760-2_1760-1del	rs2538480268
NM_020975.6(RET):c.1817A>G (p.Tyr606Cys)	rs377767395
NM_020975.6(RET):c.1831T>C (p.Cys611Arg)	rs377767391
NM_020975.6(RET):c.1879+1del	rs2538484349
NM_020975.6(RET):c.1888T>A (p.Cys630Ser)	rs377767404
NM_020975.6(RET):c.1947G>A (p.Ser649=)	rs377767412
NM_020975.6(RET):c.2370_2371delinsTC (p.Leu790_Tyr791delinsPheHis)	rs2538550904
NM_020975.6(RET):c.2617C>T (p.Arg873Trp)	rs1838178513
NM_020975.6(RET):c.3148C>T (p.Arg1050Ter)	rs767479170

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