List of variants in gene COL2A1 reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_001844.5(COL2A1):c.25A>T (p.Thr9Ser)	rs3803183	0.75794
NM_001844.5(COL2A1):c.85+18C>G	rs3803184	0.75547
NM_001844.5(COL2A1):c.3991G>A (p.Val1331Ile)	rs12721427	0.05396
NM_001844.5(COL2A1):c.4318-91C>T	rs61048429	0.05196
NM_001844.5(COL2A1):c.2094+7A>G	rs17801742	0.05167
NM_001844.5(COL2A1):c.1836T>C (p.Gly612=)	rs41317939	0.05124
NM_001844.5(COL2A1):c.4068C>T (p.Gly1356=)	rs17122498	0.04377
NM_001844.5(COL2A1):c.426A>T (p.Glu142Asp)	rs34392760	0.03719
NM_001844.5(COL2A1):c.3597+62C>T	rs73297147	0.02515
NM_001844.5(COL2A1):c.*4C>T	rs41272773	0.02262
NM_001844.5(COL2A1):c.3328-20G>T	rs73297150	0.02225
NM_001844.5(COL2A1):c.610-7G>A	rs7967258	0.01915
NM_001844.5(COL2A1):c.1266+7G>A	rs41317915	0.01359
NM_001844.5(COL2A1):c.1680+17C>T	rs115270781	0.01302
NM_001844.5(COL2A1):c.2484G>C (p.Gly828=)	rs1793940	0.01213
NM_001844.5(COL2A1):c.1545C>A (p.Arg515=)	rs41317925	0.01027
NM_001844.5(COL2A1):c.213C>T (p.Asp71=)	rs112469769	0.00730
NM_001844.5(COL2A1):c.708+8C>T	rs41317893	0.00720
NM_001844.5(COL2A1):c.2160C>A (p.Gly720=)	rs145704340	0.00654
NM_001844.5(COL2A1):c.4104C>T (p.Pro1368=)	rs12721379	0.00478
NM_001844.5(COL2A1):c.1221C>T (p.Ser407=)	rs150865922	0.00456
NM_001844.5(COL2A1):c.1221+20G>C	rs41317913	0.00432
NM_001844.5(COL2A1):c.4449G>A (p.Pro1483=)	rs41272771	0.00357
NM_001844.5(COL2A1):c.2334C>T (p.Ala778=)	rs35504014	0.00278
NM_001844.5(COL2A1):c.85+10C>G	rs769941617	0.00128
NM_001844.5(COL2A1):c.2095-4G>A	rs111570218	0.00089
NM_001844.5(COL2A1):c.1176C>T (p.Arg392=)	rs201575114	0.00051
NM_001844.5(COL2A1):c.1581+16G>A	rs182598943	0.00024
NM_001844.5(COL2A1):c.246C>T (p.Phe82=)	rs142161948	0.00014
NM_001844.5(COL2A1):c.2464-19A>C	rs200042189	0.00009

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