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rs267608099(AGTG;AGTG)

From SNPedia
(Redirected from I5037859(I;I))
common in clinvar
Is agenotype
ofrs267608099
GeneMSH6
Chromosome2
Position47,804,987
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;AGTG) 6 Lynch syndrome, pathogenic mutation
(AGTG;AGTG) 0 common in clinvar
(GAGT;GAGT) 0 common in clinvar