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rs63751449(A;A)

From SNPedia

common in clinvar
Is agenotype
ofrs63751449
GeneMSH2
Chromosome2
Position47,410,181
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;-) 7 Lynch syndrome; hereditary nonpolyposis colorectal cancer-1
(-;A) 3.5 carrier of a Lynch syndrome allele
(A;A) 0 common in clinvar
(I;I) 0