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. 2022 Jan 24;119(5):e2108672119. doi: 10.1073/pnas.2108672119

Table 2.

Genome-wide significant association signals in early-onset myasthenia gravis

Chr Position (SNPid) Nearest gene EA/OA Cohort EAF OR (95%CI) P
6 31442744 (rs3093958) HCP5/MICA G/A All 0.245/0.094 4.49 (3.62–5.57) 3.97 × 10−42
M 0.117/0.094 1.90 (1.28–2.82) 1.47 × 10−3
F 0.290/0.094 6.39 (5.01–8.14) 7.46 × 10−51
11 116158033 (rs73007767) LINC02151 G/T All 0.129/0.087 1.85 (1.48–2.30) 4.36 × 10−8
M 0.133/0.087 1.80 (1.26–2.56) 1.14 × 10−3
F 0.128/0.087 1.81 (1.42–2.32) 2.17 × 10−6

Positions are in build hg38; Chr, chromosome; EA/OA, effect allele/other allele; EAF, effect allele frequency in cases and controls; meta-analysis is based on early-onset myasthenia gravis cases from the US and Italian cohorts (595 cases and 2,718 controls).