List of variants in gene RET reported as pathogenic for digestive system disorder

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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: 23

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.2372A>T (p.Tyr791Phe)	rs77724903	0.00178
NM_020975.6(RET):c.2410G>A (p.Val804Met)	rs79658334	0.00022
NM_020975.6(RET):c.1998G>T (p.Lys666Asn)	rs146646971	0.00003
NM_020975.6(RET):c.1826G>A (p.Cys609Tyr)	rs77939446	0.00001
NM_020975.6(RET):c.1900T>C (p.Cys634Arg)	rs75076352	0.00001
NM_020975.6(RET):c.1996A>G (p.Lys666Glu)	rs143795581	0.00001
NM_020975.6(RET):c.2370G>T (p.Leu790Phe)	rs75030001	0.00001
NM_020975.6(RET):c.2671T>G (p.Ser891Ala)	rs75234356	0.00001
NM_020975.6(RET):c.111G>A (p.Trp37Ter)	rs1564489315
NM_020975.6(RET):c.1196C>T (p.Pro399Leu)	rs1554818362
NM_020975.6(RET):c.1280_1281del (p.Val427fs)	rs1564494285
NM_020975.6(RET):c.1852T>G (p.Cys618Gly)	rs76262710
NM_020975.6(RET):c.1858T>C (p.Cys620Arg)	rs77316810
NM_020975.6(RET):c.1858T>G (p.Cys620Gly)	rs77316810
NM_020975.6(RET):c.1859G>A (p.Cys620Tyr)	rs77503355
NM_020975.6(RET):c.1947G>A (p.Ser649=)	rs377767412
NM_020975.6(RET):c.1998G>C (p.Lys666Asn)	rs146646971
NM_020975.6(RET):c.2753T>C (p.Met918Thr)	rs74799832
NM_020975.6(RET):c.2865dup (p.Pro956fs)	rs1564500612
NM_020975.6(RET):c.3143del (p.Leu1048fs)	rs1564501934
NM_020975.6(RET):c.712G>T (p.Glu238Ter)	rs1588866040
NM_020975.6(RET):c.860G>A (p.Arg287Gln)	rs1564491460
NM_020975.6(RET):c.99_100del (p.Asp34fs)	rs1837613320

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