List of variants in gene RET reported as benign for Multiple endocrine neoplasia, type 2a

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: 32

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.3187+47T>C	rs2075912	0.84041
NM_020975.6(RET):c.2307G>T (p.Leu769=)	rs1800861	0.79547
NM_020975.6(RET):c.135A>G (p.Ala45=)	rs1800858	0.79274
NM_020975.6(RET):c.1296A>G (p.Ala432=)	rs1800860	0.74268
NM_020975.6(RET):c.867+48A>G	rs2435352	0.37996
NM_020975.6(RET):c.73+53G>A	rs12267460	0.37428
NM_020975.6(RET):c.337+9G>A	rs2435351	0.20641
NM_020975.6(RET):c.2712C>G (p.Ser904=)	rs1800863	0.17043
NM_020975.6(RET):c.2071G>A (p.Gly691Ser)	rs1799939	0.16640
NM_020975.6(RET):c.*1969T>C	rs3026785	0.04255
NM_020975.6(RET):c.1264-5C>T	rs9282835	0.02749
NM_020975.6(RET):c.2944C>T (p.Arg982Cys)	rs17158558	0.01567
NM_020975.6(RET):c.868-18G>A	rs57098408	0.01028
NM_020975.6(RET):c.166C>A (p.Leu56Met)	rs145633958	0.00310
NM_020975.6(RET):c.833C>A (p.Thr278Asn)	rs35118262	0.00056
NM_020975.6(RET):c.1946C>T (p.Ser649Leu)	rs148935214	0.00039
NM_020975.6(RET):c.1529C>T (p.Ala510Val)	rs201745826	0.00019
NM_020975.6(RET):c.1017G>A (p.Ser339=)	rs369810881	0.00014
NM_020975.6(RET):c.1893C>T (p.Asp631=)	rs55846256	0.00013
NM_020975.6(RET):c.1530C>T (p.Ala510=)	rs553492964	0.00009
NM_020975.6(RET):c.2409C>T (p.Ile803=)	rs535051804	0.00006
NM_020975.6(RET):c.3188-9C>T	rs551159582	0.00005
NM_020975.6(RET):c.1118C>T (p.Ala373Val)	rs546866208	0.00004
NM_020975.6(RET):c.2298G>A (p.Pro766=)	rs140658743	0.00003
NM_020975.6(RET):c.539G>A (p.Arg180Gln)	rs370736139	0.00003
NM_020975.6(RET):c.1941C>T (p.Ile647=)	rs75225191	0.00002
NM_020975.6(RET):c.2070C>T (p.Ser690=)	rs201550433	0.00001
NM_020975.6(RET):c.2715C>T (p.Tyr905=)	rs755023496	0.00001
NM_020975.6(RET):c.2393-14C>T	rs144269978
NM_020975.6(RET):c.2523G>A (p.Pro841=)	rs56195026
NM_020975.6(RET):c.2765C>A (p.Ser922Tyr)	rs377767432
NM_020975.6(RET):c.74-50G>T	rs766786245

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