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rs63750198(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs63750198
GeneMLH1
Chromosome3
Position37,014,509
Merged fromRs121912956
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 4 possible Lynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC2)
(A;C) 3 possible Lynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC2)
(C;C) 0 common in clinvar