Table 1 |.
SNP | Position (hg38) | Closest gene | Minor allele | MAF | Ref. |
---|---|---|---|---|---|
rs115684722 | 1:23,224,0417 | SIPA1L2 | T | 0.003 | 36 |
rs2633682 | 3:104,690,364 | ALCAM | A | 0.338 | 36 |
rs168193 | 3:5,260,392 | EDEM1 | G | 0.267 | 36 |
rs145848414 | 5:174,587,111 | NSG2/MSX2 | A | 0.0416 | 38 |
rs184179037 | 5:37,483,838 | WDR70 | T | 0.0008 | 36 |
rs7748513 | 6:41,160,234 | TREM2 a | A | 0.459 | 36 |
rs112404845 | 7:51,510,325 | COBL | T | 0.01 | 206 |
rs569584007 | 11:43,145,292 | API5 b | G | 0.0023 | 36 |
rs115816806 | 11:76,830,796 | ACER3 | G | 0.0083 | 36 |
rs75739461 | 12:18,318,612 | PIK3C2G | A | 0.0151 | 36 |
rs9516245 | 13:93,507,547 | GPC6 | C | 0.0189 | 36 |
rs570487962 | 15:97,449,455 | ARRDC4/IGF1R | C | 0.0008 | 36 |
rs79537509 | 16:8,238,399 | RBFOX1 a | A | 0.007 | 36 |
rs115550680 | 19:1,050,421 | ABCA7 a | G | 0.0681 | 38 |
rs157591 | 19:44,920,677 | APOE a | A | 0.1422 | 38 |
rs3745495 | 19:50,021,075 | VRK3 c | G | 0.0877 | 36 |
A P value cut-off of ≤10−7 indicates loci suggestive of genome-wide significance. GWAS, genome-wide association study; hg38, Genome Reference Consortium Human Build 38; MAF, minor allele frequency; SNP, single-nucleotide polymorphism.
Locus is also observed in non-Hispanic white individuals.
5 Mb apart from but not in linkage disequilibrium with CELF1/SPI1 locus observed in non-Hispanic white individuals16.
1.7 Mb apart from but not in linkage disequilibrium with CD33 observed in non-Hispanic white individuals17.