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rs63751077(C;C)

From SNPedia
(Redirected from I5901102(C;C))
common in clinvar
Is agenotype
ofrs63751077
GeneMSH6
Chromosome2
Position47,796,035
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;C) 6 Lynch syndrome, pathogenic mutation
(C;C) 0 common in clinvar