List of variants in gene RET reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.1296A>G (p.Ala432=)	rs1800860	0.74268
NM_020975.6(RET):c.337+9G>A	rs2435351	0.20840
NM_020975.6(RET):c.2307= (p.Leu769=)	rs1800861	0.20453
NM_020975.6(RET):c.2608-24G>A	rs2472737	0.20232
NM_020975.6(RET):c.2712C>G (p.Ser904=)	rs1800863	0.17043
NM_020975.6(RET):c.2071G>A (p.Gly691Ser)	rs1799939	0.16948
NM_020975.6(RET):c.2508C>T (p.Ser836=)	rs1800862	0.03791
NM_020975.6(RET):c.1264-5C>T	rs9282835	0.02749
NM_020975.6(RET):c.2944C>T (p.Arg982Cys)	rs17158558	0.01651
NM_020975.6(RET):c.868-18G>A	rs57098408	0.00960
NM_020975.6(RET):c.375C>A (p.Val125=)	rs1800859	0.00877
NM_020975.6(RET):c.468C>T (p.Ala156=)	rs141290380	0.00162
NM_020975.6(RET):c.833C>A (p.Thr278Asn)	rs35118262	0.00056
NM_020975.6(RET):c.2037C>T (p.Pro679=)	rs55862116	0.00039
NM_020975.6(RET):c.1050C>T (p.Thr350=)	rs142188675	0.00029
NM_020975.6(RET):c.2088G>A (p.Ser696=)	rs150329150	0.00023

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