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rs1800937(C;T)

From SNPedia
benign polymorphism
Is agenotype
ofrs1800937
GeneMSH6
Chromosome2
Position47,798,625
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;C) 6 Lynch syndrome, pathogenic mutation
(C;C) 0 common in clinvar
(C;G) 6 Lynch syndrome, pathogenic mutation
(C;T) 0 benign polymorphism
(T;T) 0 benign polymorphism