Skip to main content

Advertisement

Table 2 Top variants from meta-analysis lookup in humanin-like nuclear isoform gene regions and with 50 kb flanking region in both directions

From: Genetic variants in humanin nuclear isoform gene regions show no association with coronary artery disease

GeneTop SNP (with flanking)AllelesaEAFORP-valueTop SNP (no flanking)AllelesEAFOR (95% CI)P-value
(95% CI)
MTRNR2L1rs56173058G/A0.981.08 (1.01–1.16)0.034rs79253571C/T0.981.04 (0.98–1.11)0.17
MTRNR2L2rs6151662G/A0.951.06 (1.02–1.11)0.0037rs150977859T/C0.0531.02 (0.98–1.06)0.3
MTRNR2L3rs117764606T/C0.0141.11 (1.03–1.20)0.0074rs113906620T/C0.0251.04 (0.99–1.10)0.14
MTRNR2L4rs75856110T/C0.00261.34 (1.08–1.67)0.0086rs72776357C/A0.881.01 (0.98–1.03)0.48
MTRNR2L5rs72788864G/A0.051.05 (1.01–1.10)0.016rs11004929C/T0.371.01 (1.00–1.03)0.1
MTRNR2L6rs34587783T/C0.931.04 (1.01–1.08)0.0087rs58504986A/G0.561.01 (1.00–1.03)0.14
MTRNR2L7rs148910803C/G0.991.12 (1.00–1.24)0.047rs2208320G/T0.341.01 (0.99–1.02)0.55
MTRNR2L8rs76836360T/C0.000163.52 (1.48–8.37)0.0044rs7350542G/A0.191.02 (0.99–1.04)0.15
MTRNR2L9rs60678216G/A0.0351.05 (1.01–1.10)0.026rs6915206C/T0.41 (0.99–1.02)0.59
MTRNR2L10rs5914251C/A0.141.02 (0.99–1.05)0.15rs10521478A/G0.571.01 (0.98–1.04)0.62
MTRNR2L11rs202137689TG/-0.031.06 (1.01–1.11)0.029rs12093187C/T0.0291.04 (0.98–1.10)0.25
MTRNR2L12rs78077066T/G0.011.12 (1.02–1.23)0.015rs12106821A/G0.0371.02 (0.95–1.10)0.52
MTRNR2L13rs10020248C/T0.211.03 (1.01–1.05)0.013rs78083998G/C0.0311.05 (1.10–1.00)0.042
  1. aEffect allele/other allele