List of variants in gene COL9A3 reported as uncertain significance by Genome Diagnostics Laboratory, The Hospital for Sick Children

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_001853.4(COL9A3):c.388G>A (p.Gly130Ser)	rs139401633	0.00096
NM_001853.4(COL9A3):c.245C>T (p.Pro82Leu)	rs199653123	0.00011
NM_001853.4(COL9A3):c.275G>C (p.Gly92Ala)	rs1991064282
NM_001853.4(COL9A3):c.337G>C (p.Gly113Arg)	rs574865366
NM_001853.4(COL9A3):c.422C>G (p.Pro141Arg)	rs141879928

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