List of variants in gene combination LOC111365177, LOC113219432, LOC126860158, MET reported as uncertain significance for adenocarcinoma

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: 1

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HGVS	dbSNP	gnomAD frequency
NM_001127500.2(MET):c.1528-?_*2262dup4962

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