ClinVar Miner

List of variants in gene combination COL6A2, FTCD reported as benign by Preventiongenetics, part of Exact Sciences

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Total variants: 6
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HGVS dbSNP gnomAD frequency
NM_001849.4(COL6A2):c.2979C>T (p.Arg993=) rs6652 0.14487
NM_001849.4(COL6A2):c.2724A>G (p.Thr908=) rs9977394 0.13855
NM_001849.4(COL6A2):c.2803G>A (p.Gly935Arg) rs35548026 0.08193
NM_001849.4(COL6A2):c.3043A>C (p.Ile1015Leu) rs11910483 0.02152
NM_001849.4(COL6A2):c.2592G>A (p.Thr864=) rs1042930 0.01149
NM_001849.4(COL6A2):c.2697G>T (p.Thr899=) rs11554669

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