List of variants in gene RET reported as likely pathogenic for Multiple endocrine neoplasia type 2A

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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: 13

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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.1522+35C>T	rs377130948	0.00011
NM_020975.6(RET):c.1998G>T (p.Lys666Asn)	rs146646971	0.00003
NM_020975.6(RET):c.2392+19T>C	rs778745375	0.00003
NM_020975.6(RET):c.1996A>G (p.Lys666Glu)	rs143795581	0.00001
NM_020975.6(RET):c.2752A>G (p.Met918Val)	rs377767442	0.00001
NM_020975.6(RET):c.1998G>C (p.Lys666Asn)	rs146646971
NM_020975.6(RET):c.1998delinsTTCT (p.Lys666delinsAsnSer)	rs377767440
NM_020975.6(RET):c.2284+13C>T
NM_020975.6(RET):c.2284+19C>T
NM_020975.6(RET):c.2304G>T (p.Glu768Asp)	rs78014899
NM_020975.6(RET):c.2370G>C (p.Leu790Phe)	rs75030001
NM_020975.6(RET):c.2711C>T (p.Ser904Phe)	rs267607011

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