List of variants in gene RET reported as uncertain significance by Revvity Omics, Revvity

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.1699G>A (p.Asp567Asn)	rs147219360	0.00014
NM_020975.6(RET):c.3199C>T (p.Pro1067Ser)	rs775583354	0.00004
NM_020975.6(RET):c.701G>A (p.Arg234Gln)	rs756216318	0.00001
NM_020975.6(RET):c.1141T>C (p.Phe381Leu)	rs781362020
NM_020975.6(RET):c.1146G>A (p.Gln382=)	rs770637118
NM_020975.6(RET):c.209A>G (p.Gln70Arg)	rs1329573334

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