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rs267608120(CAAG;CAAG)

From SNPedia
(Redirected from Rs267608120(GCAAG;GCAAG))
common in clinvar
Is agenotype
ofrs267608120
GeneFBXO11, MSH6
Chromosome2
Position47,806,609
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;CAAG) 6 Lynch syndrome, pathogenic mutation
(AAGC;AAGC) 0 common in clinvar
(CAAG;CAAG) 0 common in clinvar