ClinVar Miner

List of variants in gene RET reported as uncertain significance by Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein

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.667G>A (p.Val223Met)	rs587780815	0.00001
NM_020975.6(RET):c.50T>C (p.Leu17Pro)	rs1837066964

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