List of variants in gene COL6A2 reported as uncertain significance for See cases

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001849.4(COL6A2):c.1562G>A (p.Arg521Gln)	rs367693258	0.00001
NM_001849.4(COL6A2):c.179A>C (p.Gln60Pro)	rs147892526
NM_001849.4(COL6A2):c.2737T>G (p.Ser913Ala)	rs2078770367

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