List of variants in gene RET reported as benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 13

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HGVS	dbSNP	gnomAD frequency
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.166C>A (p.Leu56Met)	rs145633958	0.00310
NM_020975.6(RET):c.1336G>C (p.Gly446Arg)	rs115423919	0.00238
NM_020975.6(RET):c.2372A>T (p.Tyr791Phe)	rs77724903	0.00178
NM_020975.6(RET):c.468C>T (p.Ala156=)	rs141290380	0.00173
NM_020975.6(RET):c.1197G>A (p.Pro399=)	rs148371113	0.00108
NM_020975.6(RET):c.262A>G (p.Ile88Val)	rs141679950	0.00056
NM_020975.6(RET):c.2037C>T (p.Pro679=)	rs55862116	0.00039
NM_020975.6(RET):c.1158G>A (p.Ala386=)	rs373540097	0.00034
NM_020975.6(RET):c.2052G>A (p.Pro684=)	rs145122337	0.00019
NM_020975.6(RET):c.2538C>T (p.Leu846=)	rs201816539	0.00001
NM_020975.6(RET):c.960C>T (p.Pro320=)	rs756761746

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