ClinVar Miner

List of variants reported as likely benign for papillary adenocarcinoma by Labcorp Genetics (formerly Invitae), Labcorp

Included ClinVar conditions (8):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000245.4(MET):c.-7T>C	rs863224376	0.00001
NM_000245.4(MET):c.3867C>T (p.Thr1289=)	rs587780532
NM_000245.4(MET):c.51C>T (p.Thr17=)	rs1584875653

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