List of variants in gene RET reported as uncertain significance by Genetics and Molecular Pathology, SA Pathology

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.1531G>A (p.Glu511Lys)	rs201553718	0.00018
NM_020975.6(RET):c.1699G>A (p.Asp567Asn)	rs147219360	0.00014
NM_020975.6(RET):c.2556C>G (p.Ile852Met)	rs377767426	0.00011
NM_020975.6(RET):c.143C>T (p.Thr48Met)	rs1427186016
NM_020975.6(RET):c.1921G>C (p.Ala641Pro)	rs377767411

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