SNP | Physical location | Function | Allele | Minor allele | Minor allele frequency |
---|---|---|---|---|---|
rs10490923 | 10:122454735 | Intron variant, missense | A/G | A | 0.022 |
rs10490924 | 10:122454932 | Intron variant, missense | G/T | T | 0.402 |
rs2736911 | 10:122454839 | Intron variant, stop gained | C/T | T | 0.122 |
rs2736912 | 10:122456078 | Intron variant | C/T | T | 0.081 |