Severe Infantile Form

Other 116 variants 1 gene

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Associated Genes (1)
Associated Variants (116)
RSID Gene Risk Allele Odds Ratio Evidence
RS771406546 CPT2 — — strong
RS369369333 CPT2 — — strong
RS1557719455 CPT2 — — strong
RS138855128 CPT2 — — strong
RS201966320 CPT2 — — strong
RS200252755 CPT2 — — strong
RS201745292 CPT2 — — strong
RS908749525 CPT2 — — strong
RS1645445189 CPT2 — — strong
RS752468216 CPT2 — — strong
RS539239516 CPT2 — — strong
RS372313619 CPT2 — — strong
RS2100254724 CPT2 — — strong
RS1572385947 CPT2 — — strong
RS1645443275 CPT2 — — strong
RS780286639 CPT2 — — strong
RS1446745791 CPT2 — — strong
RS973697337 CPT2 — — strong
RS1287533399 CPT2 — — strong
RS2525558530 CPT2 — — strong
RS2525566830 CPT2 — — strong
RS2525570359 CPT2 — — strong
RS1416248797 CPT2 — — strong
RS2525558154 CPT2 — — strong
RS796051942 CPT2 — — strong
RS1553169720 CPT2 — — strong
RS1553170033 CPT2 — — strong
RS1553169598 CPT2 — — strong
RS762366252 CPT2 — — strong
RS1553169771 CPT2 — — strong
RS1553169799 CPT2 — — strong
RS1553169973 CPT2 — — strong
RS1553170029 CPT2 — — strong
RS1553168850 CPT2 — — strong
RS1553169106 CPT2 — — strong
RS756839691 CPT2 — — strong
RS1553169666 CPT2 — — strong
RS1187631754 CPT2 — — strong
RS1229197873 CPT2 — — strong
RS1317793581 CPT2 — — strong
RS1553169726 CPT2 — — strong
RS371971257 CPT2 — — strong
RS1553170005 CPT2 — — strong
RS1553169813 CPT2 — — strong
RS1553170006 CPT2 — — strong
RS770734793 CPT2 — — strong
RS760255368 CPT2 — — strong
RS764849762 CPT2 — — strong
RS1557718075 CPT2 — — strong
RS1009503062 CPT2 — — strong
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