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rs63751598(A;A)

From SNPedia
common in clinvar
Is agenotype
ofrs63751598
GeneMLH1
Chromosome3
Position37,017,598
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 0 common in clinvar
(A;C) 6 Lynch syndrome, pathogenic mutation
(A;G) 6 Lynch syndrome, pathogenic mutation