List of variants in gene RET reported as uncertain significance for central nervous system neoplasm

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.2657G>A (p.Arg886Gln)	rs373594744	0.00009
NM_020975.6(RET):c.604G>A (p.Val202Met)	rs751572082	0.00006

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