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rs63750690(GGACC;GGACC)

From SNPedia
common in clinvar
Is agenotype
ofrs63750690
GeneMSH2
Chromosome2
Position47,412,485
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(GGACC;GGACC) 0 common in clinvar
(GGACC;TTA) 6 Lynch syndrome, pathogenic mutation