List of variants in gene RET reported as uncertain significance by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.1946C>T (p.Ser649Leu)	rs148935214	0.00039
NM_020975.6(RET):c.785T>C (p.Val262Ala)	rs139790943	0.00024
NM_020975.6(RET):c.1531G>A (p.Glu511Lys)	rs201553718	0.00018
NM_020975.6(RET):c.1063+9G>A	rs765463636	0.00014
NM_020975.6(RET):c.1699G>A (p.Asp567Asn)	rs147219360	0.00014
NM_020975.6(RET):c.1522+35C>T	rs377130948	0.00011
NM_020975.6(RET):c.2081G>A (p.Arg694Gln)	rs141185224	0.00008
NM_020975.6(RET):c.604G>A (p.Val202Met)	rs751572082	0.00006
NM_020975.6(RET):c.3148C>G (p.Arg1050Gly)	rs767479170	0.00001
NM_020975.6(RET):c.3314C>T (p.Ala1105Val)	rs532862288	0.00001
NM_020975.6(RET):c.544C>A (p.Pro182Thr)	rs775086466	0.00001
NM_020975.6(RET):c.937C>T (p.Arg313Trp)	rs1057521089	0.00001
NM_020975.6(RET):c.3182T>C (p.Leu1061Pro)	rs536486113
NM_020975.6(RET):c.3237_3238del (p.Arg1079fs)	rs1060499895
NM_020975.6(RET):c.947G>T (p.Ser316Ile)	rs1060499894

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