List of variants in gene COL9A1 reported as uncertain significance for not specified

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001851.6(COL9A1):c.876+2dup	rs672601329	0.00030
NM_001851.6(COL9A1):c.1423G>A (p.Gly475Ser)	rs143320197	0.00024
NM_001851.6(COL9A1):c.2629C>T (p.Arg877Ter)	rs758388716	0.00001
NM_001851.6(COL9A1):c.1557+6T>C	rs1057518423
NM_001851.6(COL9A1):c.2504-11A>G
NM_001851.6(COL9A1):c.913-5C>G	rs763816689

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