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rs63750261(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs63750261
GenePMS2
Chromosome7
Position5,999,110
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;G) 6 Lynch syndrome
(C;C) 0 common in clinvar
(C;T) 6 Lynch syndrome, pathogenic mutation