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rs139075637(A;T)

From SNPedia
Variant of uncertain significance wrt colon cancer; could be benign
Is agenotype
ofrs139075637
GenePOLE
Chromosome12
Position132,676,594
mentionedby
Magnitude1
ReputeBad
Geno Mag Summary
(A;A) 0 common/normal
(A;T) 1 Variant of uncertain significance wrt colon cancer; could be benign

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