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rs267607706(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs267607706
GeneEPM2AIP1, MLH1
Chromosome3
Position36,993,661
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;C) 6 Lynch syndrome
(C;C) 0 common in clinvar
(C;G) 6 Lynch syndrome, pathogenic mutation