Associated SNPs at chromosome 2 and 5 loci
Chromosome* . | Position* . | SNP rs ID . | . | Minor allele . | Major allele . | MAF cases . | MAF controls . | P . | Odds ratio (95% CI) . | Global MAF . | YRI MAF . | CEU MAF . |
---|---|---|---|---|---|---|---|---|---|---|---|---|
2 | 15 252,558 | rs66516066 | Imputed | T | A | 0.06 | 0.23 | 2.01e-08* | 0.21 (0.11-0.37) | 0.07 | 0.11 | 0.08 |
2 | 15 234,153 | rs56737264 | Genotyped | G | A | 0.09 | 0.27 | 1.56e-07 | 0.28 (0.17-0.46) | 0.07 | 0.15 | 0.07 |
2 | 15 242,283 | rs67088901 | Genotyped | A | G | 0.08 | 0.23 | 6.36e-07 | 0.28 (0.16-0.47) | 0.07 | 0.13 | 0.08 |
5 | 159 277,285 | rs75853687 | Genotyped | A | G | 0.12 | 0.01 | 8.36e-08 | 16.46 (3.91-69.26) | 0.02 | 0.10 | — |
5 | 159 285,569 | rs116416070 | Imputed | T | C | 0.11 | 0.00 | 1.13e-07 | 28.76 (3.89-212.8) | 0.01 | 0.10 | — |
5 | 159 285,922 | rs114221476 | Imputed | A | G | 0.11 | 0.00 | 1.13e-07 | 28.76 (3.89-212.8) | 0.01 | 0.10 | — |
Chromosome* . | Position* . | SNP rs ID . | . | Minor allele . | Major allele . | MAF cases . | MAF controls . | P . | Odds ratio (95% CI) . | Global MAF . | YRI MAF . | CEU MAF . |
---|---|---|---|---|---|---|---|---|---|---|---|---|
2 | 15 252,558 | rs66516066 | Imputed | T | A | 0.06 | 0.23 | 2.01e-08* | 0.21 (0.11-0.37) | 0.07 | 0.11 | 0.08 |
2 | 15 234,153 | rs56737264 | Genotyped | G | A | 0.09 | 0.27 | 1.56e-07 | 0.28 (0.17-0.46) | 0.07 | 0.15 | 0.07 |
2 | 15 242,283 | rs67088901 | Genotyped | A | G | 0.08 | 0.23 | 6.36e-07 | 0.28 (0.16-0.47) | 0.07 | 0.13 | 0.08 |
5 | 159 277,285 | rs75853687 | Genotyped | A | G | 0.12 | 0.01 | 8.36e-08 | 16.46 (3.91-69.26) | 0.02 | 0.10 | — |
5 | 159 285,569 | rs116416070 | Imputed | T | C | 0.11 | 0.00 | 1.13e-07 | 28.76 (3.89-212.8) | 0.01 | 0.10 | — |
5 | 159 285,922 | rs114221476 | Imputed | A | G | 0.11 | 0.00 | 1.13e-07 | 28.76 (3.89-212.8) | 0.01 | 0.10 | — |
SNP rs66516066 on chromosome 2 surpasses genome wide significance. Chromosome 5 SNPs are not observed in CEU cohort of 1000 genomes. Italics differentiate genotyped from imputed (inferred) variants.
All positions are relative to GRCh37/hg19 human genome build.