ClinVar Miner

List of variants in gene COLQ reported as benign by Preventiongenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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HGVS dbSNP gnomAD frequency
NM_005677.4(COLQ):c.600+40G>A rs2305616 0.46616
NM_005677.4(COLQ):c.394-27C>G rs2305612 0.38369
NM_005677.4(COLQ):c.529-23A>G rs924812 0.37081
NM_005677.4(COLQ):c.528+22A>G rs3816526 0.37075
NM_005677.4(COLQ):c.1298+35C>A rs1077827 0.11659
NM_005677.4(COLQ):c.934A>G (p.Ser312Gly) rs6782980 0.05224
NM_005677.4(COLQ):c.366+7A>G rs750387 0.04329
NM_005677.4(COLQ):c.556-15A>G rs57376327 0.02543
NM_005677.4(COLQ):c.1248C>T (p.Asp416=) rs55866379 0.02373
NM_005677.4(COLQ):c.1298+34T>A rs71308146
NM_005677.4(COLQ):c.1338C>A (p.Ile446=) rs73818504

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