rs731236
rs731236 · 4 retained evidence mentions
Source-grounded findings
Supporting evidence
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| variant | rs731236 | “The strongest linkage disequilibrium was observed between rs79785232 (ApaI) and rs731236 (TaqI) polymorphisms (r2=.83), followed by rs2228570 (FokI) and rs1544410 (BsmI) polymorphisms (r2=.53).” | 0.90 | hgvs_regex_v1 |
| variant | rs731236 | “The aim of this study is to investigate the possible association of two identified mutations ApaI (rs7975232) and TaqI (rs731236).” | 0.90 | hgvs_regex_v1 |
| variant | rs731236 | “RESULTS: For the ApaI single-nucleotide polymorphism (SNP) (rs7975232), only the heterozygous (Aa) genotype increased the risk of CRC (OR = 3.4, RR = 2.3, and P < 0.0001), whereas the TaqI SNP (rs731236) carriers with either the heterozygous (Tt) or homozygous (tt) genotype displayed an increased risk for the disease (OR = 6.18, RR = 4, P < 0.0001; OR = 3, RR = 2.4, P = 0.02, respectively).” | 0.90 | hgvs_regex_v1 |
| variant | rs731236 | “Significant differences were ob served in the values of the studied parameters in rs11168276, rs11168266, rs3858733, rs121909790, rs11168265 and rs731236.” | 0.90 | hgvs_regex_v1 |