Frontotemporal Dementia And/or Amyotrophic Lateral Sclerosis 1

Neurological 65 variants 2 genes

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Associated Genes (2)
Associated Variants (65)
RSID Gene Risk Allele Odds Ratio Evidence
RS2480264648 SQSTM1 — — strong
RS201923000 SQSTM1 — — strong
RS765610848 SQSTM1 — — strong
RS2113487920 SQSTM1 — — strong
RS2113512370 SQSTM1 — — strong
RS1391182750 SQSTM1 — — strong
RS143511494 SQSTM1 — — strong
RS2113485289 SQSTM1 — — strong
RS202235745 SQSTM1 — — strong
RS771657338 SQSTM1 — — strong
RS2480264715 SQSTM1 — — strong
RS1258386028 SQSTM1 — — strong
RS1166729262 SQSTM1 — — strong
RS757212984 SQSTM1 — — strong
RS2480244186 SQSTM1 — — strong
RS2480208932 SQSTM1 — — strong
RS2113512406 SQSTM1 — — strong
RS1757759029 SQSTM1 — — strong
RS2480244231 SQSTM1 — — strong
RS373306317 SQSTM1 — — strong
RS2480199584 SQSTM1 — — strong
RS1261101487 SQSTM1 — — strong
RS2480243842 SQSTM1 — — strong
RS1758351897 SQSTM1 — — strong
RS1008679317 SQSTM1 — — strong
RS182522590 SQSTM1 — — strong
RS796051870 SQSTM1 — — strong
RS143561967 C9orf72 — — strong
RS776749939 SQSTM1 — — strong
RS200396166 SQSTM1 — — strong
RS139482113 SQSTM1 — — strong
RS886039782 SQSTM1 — — strong
RS370970067 SQSTM1 — — strong
RS878982215 SQSTM1 — — strong
RS140341924 SQSTM1 — — strong
RS141436407 SQSTM1 — — strong
RS143956614 SQSTM1 — — strong
RS1273214757 SQSTM1 — — strong
RS104893941 SQSTM1 — — strong
RS752009611 SQSTM1 — — strong
RS375495050 SQSTM1 — — strong
RS1331685476 SQSTM1 — — strong
RS1758316662 SQSTM1 — — strong
RS1757883398 SQSTM1 — — strong
RS1302810798 SQSTM1 — — strong
RS1425863340 SQSTM1 — — strong
RS1758558921 SQSTM1 — — strong
RS771966860 SQSTM1 — — strong
RS143746604 SQSTM1 — — strong
RS535606152 SQSTM1 — — strong
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