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rs587778980(GTGCCTG;GTGCCTG)

From SNPedia
common in clinvar
Is agenotype
ofrs587778980
GeneMLH1
Chromosome3
Position37,050,493
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;TGCCTGG) 6 Lynch syndrome, pathogenic mutation
(GTGCCTG;GTGCCTG) 0 common in clinvar
(TGCCTGG;TGCCTGG) 0 common/normal