Neonatal Form

Other 89 variants 1 gene

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Associated Genes (1)
Associated Variants (89)
RSID Gene Risk Allele Odds Ratio Evidence
RS539239516 CPT2 strong
RS771214714 CPT2 strong
RS200252755 CPT2 strong
RS201745292 CPT2 strong
RS908749525 CPT2 strong
RS1645445189 CPT2 strong
RS752468216 CPT2 strong
RS1212235186 CPT2 strong
RS112914907 CPT2 strong
RS909671156 CPT2 strong
RS1645411052 CPT2 strong
RS200080591 CPT2 strong
RS1374482155 CPT2 strong
RS199673903 CPT2 strong
RS372313619 CPT2 strong
RS1645443275 CPT2 strong
RS780286639 CPT2 strong
RS1446745791 CPT2 strong
RS973697337 CPT2 strong
RS2525558530 CPT2 strong
RS2525566830 CPT2 strong
RS2525570359 CPT2 strong
RS1416248797 CPT2 strong
RS2525558154 CPT2 strong
RS796051942 CPT2 strong
RS1553170005 CPT2 strong
RS373638740 CPT2 strong
RS373714948 CPT2 strong
RS1057517510 CPT2 strong
RS1057517493 CPT2 strong
RS1238901632 CPT2 strong
RS61731996 CPT2 strong
RS1553169716 CPT2 strong
RS778743524 CPT2 strong
RS1553169799 CPT2 strong
RS756839691 CPT2 strong
RS1553169720 CPT2 strong
RS371971257 CPT2 strong
RS515726173 CPT2 strong
RS1553169813 CPT2 strong
RS1553170006 CPT2 strong
RS770734793 CPT2 strong
RS760255368 CPT2 strong
RS764849762 CPT2 strong
RS1557718075 CPT2 strong
RS1009503062 CPT2 strong
RS1572385947 CPT2 strong
RS369369333 CPT2 strong
RS1557719455 CPT2 strong
RS140771069 CPT2 strong
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