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rs63751119(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs63751119
GeneMSH2
Chromosome2
Position47,478,312
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;G) 6 Lynch syndrome, pathogenic mutation
(C;G) 6 Lynch syndrome
(G;G) 0 common in clinvar