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rs63749932(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs63749932
GeneMSH2
Chromosome2
Position47,476,399
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 6 Lynch syndrome; pathogenic mutation
(T;T) 6 Lynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC1)