ClinVar Miner

List of variants in gene combination COL6A2, FTCD reported as benign by Illumina Clinical Services Laboratory,Illumina

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Gene type:
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Total variants: 9
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HGVS dbSNP
NM_001849.3(COL6A2):c.*116T>C rs3087667
NM_001849.3(COL6A2):c.*119A>G rs1043962
NM_001849.3(COL6A2):c.*158C>T rs11554666
NM_001849.3(COL6A2):c.2724A>G (p.Thr908=) rs9977394
NM_001849.3(COL6A2):c.2803G>A (p.Gly935Arg) rs35548026
NM_001849.3(COL6A2):c.2979C>T (p.Arg993=) rs6652
NM_001849.3(COL6A2):c.2980G>A (p.Ala994Thr) rs117931394
NM_001849.3(COL6A2):c.3043A>C (p.Ile1015Leu) rs11910483
NM_206965.2(FTCD):c.1470C>T (p.Gly490=) rs10432965

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