ClinVar Miner

List of variants in gene COL6A2 reported as benign for not provided

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Total variants: 76
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HGVS dbSNP
GRCh37/hg19 21q22.3(chr21:47551909-47552350)x1
GRCh37/hg19 21q22.3(chr21:47551909-47552386)x1
NC_000021.9:g.46120116del
NC_000021.9:g.46120124_46120125del
NM_001849.3(COL6A2):c.-27-149C>T
NM_001849.3(COL6A2):c.-27-89G>A
NM_001849.3(COL6A2):c.1054-100A>C
NM_001849.3(COL6A2):c.1116+200G>A
NM_001849.3(COL6A2):c.1116+221G>A
NM_001849.3(COL6A2):c.1116+32G>A rs7279347
NM_001849.3(COL6A2):c.1117-218A>T
NM_001849.3(COL6A2):c.1117-56C>G
NM_001849.3(COL6A2):c.1179+101G>T
NM_001849.3(COL6A2):c.1270-169T>C
NM_001849.3(COL6A2):c.1332+26A>G rs3737362
NM_001849.3(COL6A2):c.1332+286C>T
NM_001849.3(COL6A2):c.1332+290T>G
NM_001849.3(COL6A2):c.1332+293T>C
NM_001849.3(COL6A2):c.1332+299dup
NM_001849.3(COL6A2):c.1333-169C>T
NM_001849.3(COL6A2):c.1333-198A>C
NM_001849.3(COL6A2):c.1333-229C>T
NM_001849.3(COL6A2):c.1333-243C>T
NM_001849.3(COL6A2):c.1333-80C>T
NM_001849.3(COL6A2):c.1395+234G>A
NM_001849.3(COL6A2):c.1395+82G>A
NM_001849.3(COL6A2):c.1396-133G>C
NM_001849.3(COL6A2):c.1459-168A>G
NM_001849.3(COL6A2):c.1521+212A>G
NM_001849.3(COL6A2):c.1521+21A>G rs1077182
NM_001849.3(COL6A2):c.1522-199_1522-198insT
NM_001849.3(COL6A2):c.1522-36T>C rs9976026
NM_001849.3(COL6A2):c.1572+148C>T
NM_001849.3(COL6A2):c.1573-32C>T rs17272651
NM_001849.3(COL6A2):c.1609-155T>C
NM_001849.3(COL6A2):c.1609-163G>A
NM_001849.3(COL6A2):c.1672-177T>C
NM_001849.3(COL6A2):c.1672-24C>G rs3746995
NM_001849.3(COL6A2):c.1672-257T>C
NM_001849.3(COL6A2):c.1672-37G>T rs79205686
NM_001849.3(COL6A2):c.1734+35A>G rs55933135
NM_001849.3(COL6A2):c.1735-30A>G rs73382466
NM_001849.3(COL6A2):c.1735-72G>A
NM_001849.3(COL6A2):c.1770+4G>A rs9981981
NM_001849.3(COL6A2):c.1771-159G>A
NM_001849.3(COL6A2):c.1771-25A>G rs2839113
NM_001849.3(COL6A2):c.1817-33C>T rs2276101
NM_001849.3(COL6A2):c.1817-69T>C
NM_001849.3(COL6A2):c.1970-23G>C rs78764604
NM_001849.3(COL6A2):c.2039G>A (p.Arg680His) rs1042917
NM_001849.3(COL6A2):c.2094G>A (p.Ala698=) rs13052956
NM_001849.3(COL6A2):c.2097C>T (p.Gly699=) rs13046639
NM_001849.3(COL6A2):c.2160C>G (p.Arg720=) rs61735829
NM_001849.3(COL6A2):c.2163G>A (p.Gln721=) rs16978875
NM_001849.3(COL6A2):c.2184G>A (p.Val728=) rs2839114
NM_001849.3(COL6A2):c.2422+112C>A
NM_001849.3(COL6A2):c.2422+93T>C
NM_001849.3(COL6A2):c.2423-35C>A rs16978878
NM_001849.3(COL6A2):c.2423-83T>C
NM_001849.3(COL6A2):c.2461+2100A>C
NM_001849.3(COL6A2):c.2462-204T>C
NM_001849.3(COL6A2):c.2462-2239T>A
NM_001849.3(COL6A2):c.2462-2255C>T
NM_001849.3(COL6A2):c.2462-2299T>C
NM_001849.3(COL6A2):c.2462-2311A>G
NM_001849.3(COL6A2):c.2462-2358G>C
NM_001849.3(COL6A2):c.2462-35C>T rs7279622
NM_001849.3(COL6A2):c.663C>T (p.Pro221=) rs59531343
NM_001849.3(COL6A2):c.679G>A (p.Asp227Asn) rs35881321
NM_001849.3(COL6A2):c.714+45C>T rs2070957
NM_001849.3(COL6A2):c.714+53C>T
NM_001849.3(COL6A2):c.714+62A>G
NM_001849.3(COL6A2):c.714+9C>T rs78822624
NM_001849.3(COL6A2):c.802-250T>G
NM_001849.3(COL6A2):c.901-111C>T
NM_058174.3(COL6A2):c.1817-3dup rs149954350

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