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rs63750899(C;T)

From SNPedia

Lynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC2)
Is agenotype
ofrs63750899
GeneMLH1
Chromosome3
Position37,048,562
mentionedby
Magnitude3.5
ReputeBad
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3.5 Lynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC2)
(T;T) 4 Lynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC2)

Lynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC2); perhaps relatively mild form.