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  1. C

    My mutations..

    Both of your mutations are rare at less that 1% occurrence. R334W .05% N1303K .49% I got this information for http://www.cfmedicine.com The genetics of Cystic Fibrosis I am a carrier for R334 W. My husband is a carrier of delta F508. My baby was tested via amnio and I am waiting on the results.
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