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rs63750691(G;G)

From SNPedia

Lynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC2)
Is agenotype
ofrs63750691
GeneMLH1
Chromosome3
Position37,017,521
Merged fromRs121912964
mentionedby
Magnitude5
ReputeBad
Geno Mag Summary
(C;C) 0 common in clinvar
(C;G) 3.5 possible Lynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC2)
(G;G) 5 Lynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC2)

Lynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC2). However, be aware of the possibility of an artefact due to orientation ambiguous flips.