Table 2.
Top associated SNPs for GWAS with log maximum AST, ALT and LFT >2X ULN in LD-MTX subjects (n = 1429).
| chr | base pair | ref | alt | rs | Mapped Gene/nearest Gene | MAF | info | genotyped | association in LD-MTX subject | ||
|---|---|---|---|---|---|---|---|---|---|---|---|
| beta | se | p value | |||||||||
| log maximum AST outcome | |||||||||||
| 1 | 169,586,946 | T | C | rs2244526 | SELP | 0.1 | 0.92 | Imputed | 0.12 | 0.02 | 3.5E-07 |
| 2 | 28,804,276 | T | C | rs13421347 | PLB1 | 0.04 | 0.98 | Genotype | 0.17 | 0.03 | 4.8E-07 |
| 2 | 156,500,331 | G | A | rs72889976 | 0.04 | 0.77 | Imputed | 0.16 | 0.03 | 5.5E-07 | |
| 2 | 210,593,241 | T | G | rs71420769 | MAP2 | 0.03 | 0.78 | Imputed | 0.37 | 0.07 | 5.6E-07 |
| 4 | 67,601,162 | G | A | rs11937537 | 0.23 | 0.95 | Genotype | 0.09 | 0.02 | 1.4E-07 | |
| 12 | 131,011,393 | T | C | rs6486549 | RIMBP2 | 0.39 | 0.96 | Imputed | 0.07 | 0.01 | 9.8E-08 |
| 15 | 71,810,708 | T | C | rs59374539 | THSD4 | 0.02 | 0.99 | Genotype | 1.35 | 0.26 | 2.2E-07 |
| 17 | 65,706,413 | T | A | rs80320525 | NOL11 | 0.05 | 0.52 | Imputed | 0.81 | 0.16 | 9.4E-07 |
| 20 | 2,580,184 | C | A | rs570089265 | TMC2 | 0.02 | 0.74 | Imputed | 0.31 | 0.06 | 2.6E-07 |
| log maximum ALT outcome | |||||||||||
| 5 | 31,893,186 | TA | T | rs34950471 | PDZD2 | 0.09 | 0.77 | Imputed | 0.14 | 0.03 | 2.2E-07 |
| 9 | 1,279,510 | G | C | rs35602716 | DMRT2 | 0.02 | 0.83 | Imputed | 2.13 | 0.43 | 8.1E-07 |
| 17 | 2,707,990 | C | T | rs76993247 | RAP1GAP2 | 0.02 | 0.51 | Imputed | 0.59 | 0.09 | 5.0E-10 |
| 17 | 19,759,902 | A | C | rs28661593 | ULK2 | 0.03 | 0.70 | Imputed | 1.69 | 0.30 | 3.6E-08 |
| 18 | 8,723,770 | C | T | rs589952 | MTCL1 | 0.02 | 0.89 | Imputed | 1.14 | 0.22 | 2.0E-07 |
| 18 | 9,888,688 | A | G | rs551429 | TXNDC2 | 0.03 | 0.94 | Imputed | 1.59 | 0.30 | 1.9E-07 |
| LFT > 2X ULN outcome | |||||||||||
| 9 | 83,760,434 | A | G | rs11139045 | TLE1 | 0.03 | 0.998 | Genotype | 1.43 | 0.27 | 9.4E-08 |
| 12 | 52,994,955 | G | A | rs61747192 | KRT72 | 0.13 | 0.996 | Imputed | 0.83 | 0.17 | 9.9E-07 |
| 13 | 23,577,442 | T | C | rs77522295 | BASP1P1 | 0.04 | 0.998 | Genotype | 1.24 | 0.25 | 5.0E-07 |
Chr: chromosome; ref: reference allele; alt: alternative allele; MAF: minor allele frequency; info: imputation info score (0–1). All SNP reached suggestive significance level of 10−6. Genome wide significance was marked bold.