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rs63750347(C;T)

From SNPedia

Lynch syndrome, pathogenic mutation
Is agenotype
ofrs63750347
GeneMSH2
Chromosome2
Position47,412,522
mentionedby
Magnitude6
ReputeBad
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 6 Lynch syndrome, pathogenic mutation

see discussion at rs63750347