rs1801166(C;G)
From SNPedia
Significance unclear wrt colorectal cancer |
Is a | genotype |
of | rs1801166 |
Gene | APC |
Chromosome | 5 |
Position | 112,839,543 |
Merged from | Rs137854581 |
mentioned | by |
Magnitude | 2 |
Geno | Mag | Summary |
---|---|---|
(C;C) | 3 | increased colon cancer risk? significance is unclear |
(C;G) | 2 | Significance unclear wrt colorectal cancer |
(G;G) | 0 | common in clinvar |
Currently listed as either benign or of unknown significance in ClinVar.