List of variants in gene RET reported as uncertain significance by Breakthrough Genomics, Breakthrough Genomics

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.398G>A (p.Arg133His)	rs138265837	0.00012
NM_020975.6(RET):c.2556C>G (p.Ile852Met)	rs377767426	0.00011
NM_020975.6(RET):c.1420C>T (p.Arg474Trp)	rs775842917	0.00004
NM_020975.6(RET):c.1102C>T (p.Arg368Cys)	rs754116867	0.00001
NM_020975.6(RET):c.701G>A (p.Arg234Gln)	rs756216318	0.00001
NM_020975.6(RET):c.43_51dup (p.Leu19_Pro20insLeuLeuLeu)	rs1488217326

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