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Variant Information

Gene Interpretation
MPL chr1:43814979 chr1:43349308 c.1514G>A p.S505N Pathogenic
MPL chr1:43815008 chr1:43349337 c.1543T>G p.W515G Pathogenic
MPL chr1:43815009 chr1:43349338 c.1544G>C p.W515S Pathogenic