Table 1. Genome-wide significant associations (P-value < 5×10−8) for identified low-frequency and rare variants with EwS susceptibility using a dominant model stratified by study.
Region | Coordinate | Variant | Alleles | Minor Allele Counts (Frequency) | MH P-value | ||
---|---|---|---|---|---|---|---|
Major | Minor | Controls N = 1,346 | EwS Cases N = 733 | ||||
1q23.3 | 163530987 | rs78119607 | G | A | 4 (0.001) | 31 (0.021) | 2.38×10−11 |
20p11.23 | 21063508 | rs112837127 | G | A | 87 (0.032) | 9 (0.006) | 6.90×10−9 |
20p11.22 | 21367741 | rs2296730 | A | G | 123 (0.046) | 133 (0.091) | 4.92×10−8 |