List of variants in gene RET reported as likely pathogenic by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
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: 9

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.1971_1978del (p.His658fs)	rs2538496650
NM_020975.6(RET):c.1998G>C (p.Lys666Asn)	rs146646971
NM_020975.6(RET):c.2578_2579del (p.Gln860fs)	rs2538569005
NM_020975.6(RET):c.2599G>T (p.Glu867Ter)
NM_020975.6(RET):c.2731-2A>G	rs2132983720
NM_020975.6(RET):c.2853del (p.Tyr952fs)	rs2538615387
NM_020975.6(RET):c.664G>T (p.Glu222Ter)	rs1837729713
NM_020975.6(RET):c.706A>T (p.Lys236Ter)
NM_020975.6(RET):c.903_905dup (p.Ala301_Asp302insGlu)	rs2538402891

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