List of variants in gene COL3A1 reported as uncertain significance by Genetics and Molecular Pathology, SA Pathology

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000090.4(COL3A1):c.1733T>A (p.Met578Lys)
NM_000090.4(COL3A1):c.1754G>T (p.Gly585Val)	rs2153502692
NM_000090.4(COL3A1):c.2330G>A (p.Gly777Glu)
NM_000090.4(COL3A1):c.3836T>C (p.Val1279Ala)

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