List of variants in gene MET reported as uncertain significance by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000245.4(MET):c.2851T>C (p.Phe951Leu)	rs756670611	0.00001
NM_000245.4(MET):c.490C>G (p.Pro164Ala)	rs765759353	0.00001
NM_000245.4(MET):c.1306G>C (p.Glu436Gln)	rs200740468
NM_000245.4(MET):c.1910C>A (p.Ser637Tyr)	rs2116920387
NM_000245.4(MET):c.2209A>G (p.Ser737Gly)	rs755571526
NM_000245.4(MET):c.3658G>C (p.Val1220Leu)	rs121913670

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