List of variants in gene combination A2M, KLRG1 reported as likely benign by Labcorp Genetics (formerly Invitae), 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000014.6(A2M):c.3092G>A (p.Arg1031Gln)	rs202210880	0.00098
NM_000014.6(A2M):c.822C>T (p.Asp274=)	rs202126909	0.00079
NM_000014.6(A2M):c.360G>A (p.Val120=)	rs201901298	0.00045
NM_000014.6(A2M):c.2008C>T (p.Leu670=)	rs774667464	0.00001
NM_000014.6(A2M):c.3084T>C (p.Phe1028=)	rs769231051	0.00001

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