List of variants in gene RET reported as uncertain significance 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.1187C>T (p.Ser396Leu)	rs781646869	0.00006
NM_020975.6(RET):c.1894G>A (p.Glu632Lys)	rs377767407	0.00006
NM_020975.6(RET):c.539G>A (p.Arg180Gln)	rs370736139	0.00003
NM_020975.6(RET):c.3200C>T (p.Pro1067Leu)	rs760625882	0.00002
NM_020975.6(RET):c.1731C>G (p.Asp577Glu)	rs1554818709
NM_020975.6(RET):c.1765A>T (p.Ser589Cys)	rs786202597
NM_020975.6(RET):c.2348A>C (p.Asn783Thr)	rs587778656
NM_020975.6(RET):c.2648C>A (p.Ala883Asp)	rs1293645997

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