ClinVar Miner

List of variants in gene RET reported as likely pathogenic by Mayo Clinic Laboratories, Mayo Clinic

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.1996A>G (p.Lys666Glu)	rs143795581	0.00001
NM_020975.6(RET):c.1831T>A (p.Cys611Ser)	rs377767391

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