List of variants in gene COL9A1 reported as likely benign 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: 27

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HGVS	dbSNP	gnomAD frequency
NM_001851.6(COL9A1):c.1197+11T>C	rs73745357	0.00388
NM_001851.6(COL9A1):c.1349A>G (p.Glu450Gly)	rs77706858	0.00348
NM_001851.6(COL9A1):c.1395+14T>A	rs367801990	0.00323
NM_001851.6(COL9A1):c.1089+9C>G	rs142247988	0.00221
NM_001851.6(COL9A1):c.-50A>G	rs141436759	0.00213
NM_001851.6(COL9A1):c.1288-9A>G	rs181039243	0.00133
NM_001851.6(COL9A1):c.801+11G>C	rs200305129	0.00113
NM_001851.6(COL9A1):c.2113-19G>A	rs187218937	0.00076
NM_001851.6(COL9A1):c.1053G>A (p.Ser351=)	rs75433477	0.00067
NM_001851.6(COL9A1):c.2259+7G>T	rs373480203	0.00017
NM_001851.6(COL9A1):c.88+19A>C	rs188749185	0.00007
NM_001851.6(COL9A1):c.1342-15C>G	rs200223246	0.00003
NM_001851.6(COL9A1):c.167-11C>T	rs370460481	0.00003
NM_001851.6(COL9A1):c.1404G>A (p.Gln468=)	rs371743577	0.00002
NM_001851.6(COL9A1):c.1905C>T (p.Ser635=)	rs1057523934	0.00002
NM_001851.6(COL9A1):c.2260-20T>C	rs778775136	0.00002
NM_001851.6(COL9A1):c.1002T>A (p.Pro334=)	rs1057523730	0.00001
NM_001851.6(COL9A1):c.166+12T>C	rs886038498	0.00001
NM_001851.6(COL9A1):c.1701A>G (p.Ala567=)	rs1057523729	0.00001
NM_001851.6(COL9A1):c.2106G>A (p.Lys702=)	rs774146890	0.00001
NM_001851.6(COL9A1):c.558C>T (p.Gly186=)	rs190204582	0.00001
NM_001851.6(COL9A1):c.624A>G (p.Pro208=)	rs1554247859	0.00001
NM_001851.6(COL9A1):c.1089+11C>T	rs1554243437
NM_001851.6(COL9A1):c.1342-27CTTTT[3]	rs543377381
NM_001851.6(COL9A1):c.2113-4C>T	rs1554234147
NM_001851.6(COL9A1):c.348G>A (p.Thr116=)	rs779960146
NM_001851.6(COL9A1):c.780+14C>G	rs917108673

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