List of variants in gene COL9A3 reported as uncertain significance for Stickler syndrome

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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_001853.4(COL9A3):c.1756A>C (p.Thr586Pro)	rs145821912	0.00028
NM_001853.4(COL9A3):c.218C>T (p.Pro73Leu)	rs768298010	0.00004
NM_001853.4(COL9A3):c.1102G>A (p.Val368Ile)	rs531144768	0.00001

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