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rs63751429(C;C)

From SNPedia
Revision as of 15:14, 30 March 2014 by SNPediaBot (talk | contribs) (auto-assign normal genotype)
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common in clinvar
Is agenotype
ofrs63751429
GeneMSH2
Chromosome2
Position47,408,466
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 6 Lynch syndrome, pathogenic mutation