From: Association between CFL1gene polymorphisms and spina bifida risk in a California population
dbSNP ID | Physical Location (NCBI Build 36.1) | Nucleotide Change | Location in Gene | SNP Function Prediction§ | Observed Heterozygosity§§ | HWE p value§§ | Minor Allele Frequency (95% Confidence Interval) | Allelic Association P value | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
 |  |  |  |  | NHW | HW | NHW | HW | NHW | HW | NHW | HW | ||
 |  |  |  |  |  |  |  |  | SB | control | SB | control |  |  |
rs652021 | 10929142 | T/C | intron 2 | no known function | 0.460 | 0.438 | 0.694 | 0.292 | 0.412 (0.341,0.487) | 0.315 (0.265,0.369) | 0.395 (0.337,0.456) | 0.446 (0.383,0.512) | 0.054 | 0.293 |
rs4621 | 10929314 | A/G | exon 2 | splicing regulation (protein domain abolished) | 0.453 | 0.432 | 0.784 | 0.248 | 0.406 (0.325,0.481) | 0.309 (0.260,0.363) | 0.398 (0.339,0.459) | 0.446 (0.381,0.512) | 0.061 | 0.334 |
rs11227332 | 10929534 | A/G | intron 1 | intronic enhancer | 0.279 | 0.175 | 1.000 | 0.627 | 0.253 (0.192, 0.326) | 0.163 (0.123,0.213) | 0.169 (0.128,0.221) | 0.107 (0.072,0.156) | 0.042 | 0.057 |
rs665306 | 10929820 | C/T | intron 1 | intronic enhancer | 0.459 | 0.423 | 0.724 | 0.184 | 0.399 (0.328, 0.474) | 0.324 (0.274,0.380) | 0.394 (0.336,0.455) | 0.441 (0.378,0.507) | 0.106 | 0.339 |
rs667555 | 10930357 | G/T | intron 1 | intronic enhancer | 0.466 | 0.435 | 0.540 | 0.332 | 0.386 (0.315, 0.461) | 0.321 (0.266,0.372) | 0.391 (0.333,0.453) | 0.425 (0.361,0.492) | 0.161 | 0.509 |