ClinVar Miner

List of variants in gene RET reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.2261C>T (p.Thr754Met)	rs181856591	0.00009
NM_020975.6(RET):c.1142T>G (p.Phe381Cys)	rs139813765	0.00002

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