List of variants in gene COL9A1 reported as benign by PreventionGenetics, part of Exact Sciences

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_001851.6(COL9A1):c.1504-32T>G	rs633762	0.83978
NM_001851.6(COL9A1):c.1765-26T>C	rs519068	0.48558
NM_001851.6(COL9A1):c.1015T>C (p.Ser339Pro)	rs592121	0.46927
NM_001851.6(COL9A1):c.1720-24A>C	rs701690	0.42215
NM_001851.6(COL9A1):c.1862A>G (p.Gln621Arg)	rs1135056	0.38283
NM_001851.6(COL9A1):c.2259+32T>C	rs12191701	0.36512
NM_001851.6(COL9A1):c.975+45G>A	rs7764822	0.21907
NM_001851.6(COL9A1):c.14+39A>G	rs2242588	0.21553
NM_001851.6(COL9A1):c.89-12T>C	rs12210123	0.20825
NM_001851.6(COL9A1):c.1230+12T>C	rs6935778	0.15856
NM_001851.6(COL9A1):c.1612-26C>A	rs13219431	0.13355
NM_001851.6(COL9A1):c.1071T>C (p.Arg357=)	rs607156	0.07381
NM_001851.6(COL9A1):c.1066-36C>A	rs77357454	0.04608
NM_001851.6(COL9A1):c.876+13C>T	rs117215769	0.04499
NM_001851.6(COL9A1):c.2299A>G (p.Met767Val)	rs6910140	0.04394
NM_001851.6(COL9A1):c.1504-14T>A	rs537940	0.04260
NM_001851.6(COL9A1):c.1066-3T>C	rs16868869	0.03394
NM_001851.6(COL9A1):c.2470C>A (p.Pro824Thr)	rs34119578	0.01848
NM_001851.6(COL9A1):c.2271G>A (p.Pro757=)	rs2072650	0.01180
NM_001851.6(COL9A1):c.1666-32G>A	rs72923190	0.00751
NM_001851.6(COL9A1):c.1656T>C (p.Pro552=)	rs80251646	0.00493
NM_001851.6(COL9A1):c.1197+11T>C	rs73745357	0.00388
NM_001851.6(COL9A1):c.138G>A (p.Lys46=)	rs139361722	0.00214
NM_001851.6(COL9A1):c.904G>A (p.Gly302Ser)	rs151129325	0.00207
NM_001851.6(COL9A1):c.1569T>A (p.Gly523=)	rs150970524	0.00027
NM_001851.6(COL9A1):c.1728T>G (p.Pro576=)	rs9346373
NM_001851.6(COL9A1):c.1765-21G>A	rs2274584
NM_001851.6(COL9A1):c.2034+19T>C	rs13202029
NM_001851.6(COL9A1):c.2034+19T>G	rs13202029

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