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rs587779185(TCTG;TCTG)

From SNPedia
common in clinvar
Is agenotype
ofrs587779185
GeneMSH2
Chromosome2
Position47,414,287
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;TCTG) 6 Lynch syndrome, pathogenic mutation
(CTGT;CTGT) 0 common in clinvar
(TCTG;TCTG) 0 common in clinvar