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rs63750047(C;C)

From SNPedia

common in clinvar
Is agenotype
ofrs63750047
GeneMSH2
Chromosome2
Position47,475,066
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 6 Lynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC1)
(T;T) 6 Lynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC1)