List of variants in gene RET reported as likely pathogenic for not provided

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.1998G>T (p.Lys666Asn)	rs146646971	0.00003
NM_020975.6(RET):c.3185A>G (p.Tyr1062Cys)	rs587778659	0.00003
NM_020975.6(RET):c.1996A>G (p.Lys666Glu)	rs143795581	0.00001
NM_020975.6(RET):c.433G>A (p.Val145Ile)	rs1311922451	0.00001
NM_020975.6(RET):c.1055A>G (p.His352Arg)	rs1131691450
NM_020975.6(RET):c.1591T>C (p.Cys531Arg)	rs377767390
NM_020975.6(RET):c.1760-2_1760-1del
NM_020975.6(RET):c.1831T>A (p.Cys611Ser)	rs377767391
NM_020975.6(RET):c.229C>T (p.Arg77Cys)	rs1588862595
NM_020975.6(RET):c.2711C>T (p.Ser904Phe)	rs267607011
NM_020975.6(RET):c.2752A>G (p.Met918Val)	rs377767442
NM_020975.6(RET):c.2837C>T (p.Thr946Ile)	rs794728687
NM_020975.6(RET):c.2905C>T (p.Arg969Trp)
NM_020975.6(RET):c.3148C>T (p.Arg1050Ter)	rs767479170
NM_020975.6(RET):c.3288T>G (p.Tyr1096Ter)	rs1131691861
NM_020975.6(RET):c.443_445del (p.Ser148del)
NM_020975.6(RET):c.989G>A (p.Arg330Gln)	rs80236571

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