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rs373885654(C;C)

From SNPedia

common in clinvar
Is agenotype
ofrs373885654
GenePMS2
Chromosome7
Position5,989,799
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 5 suspected Hereditary Non-Polyposis Colorectal Cancer (HNPCC)/Lynch syndrome
(T;T) 5 suspected Constitutional Mismatch Repair Deficiency (CMMR-D) syndrome