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rs2020912(C;T)

From SNPedia

unclear if associated with hereditary nonpolyposis colorectal cancer (HNPCC5)
Is agenotype
ofrs2020912
GeneMSH6
Chromosome2
Position47,800,616
mentionedby
Magnitude2.5
ReputeBad
Geno Mag Summary
(C;T) 2.5 unclear if associated with hereditary nonpolyposis colorectal cancer (HNPCC5)
(T;T) 0 common in clinvar

This variant is probably benign, but there is a possibility it is associated with hereditary nonpolyposis colorectal cancer type-5 (HNPCC5).