Table 1 |.
Chr. | Position (bp) | ID | EA | EAF | R2 | Effect (s.e.) | P discovery | P replication | P combined | Genes |
---|---|---|---|---|---|---|---|---|---|---|
2 | 71676999 | rs10191329 | A | 0.17 | 0.97 | 0.089 (0.015) | 9.7×10−9 | 0.021 | 3.6×10−9 | DYSF–ZNF638 |
1 | 172370873 | rs149097173 | T | 0.01 | 0.94 | 0.256 (0.056) | 4.1×10−6 | 0.010 | 2.3×10−7 | DNM3–PIGC |
Effect on ARMSS score in MS patients. Two variants were genome-wide significant (bold) or suggestive in the discovery GWAS and confirmed in the replication population; two-sided P values were calculated using regression models. Pcombined represents the fixed-effects meta-analysis P value of the discovery and replication data. Chr., chromosome; bp, base pair (GRCh37); EA, effect allele; EAF, risk allele frequency; R2, imputation quality score; s.e., standard error.