Spinocerebellar Ataxia Type 19/22

Other 48 variants 2 genes

Upload your DNA to see your personal risk score for Spinocerebellar Ataxia Type 19/22.

Associated Genes (2)
Associated Variants (48)
RSID Gene Risk Allele Odds Ratio Evidence
RS144120746 KCND3 strong
RS1571939905 KCND3 strong
RS775768536 KCND3 strong
RS867628133 KCND3 strong
RS774713377 KCND3 strong
RS1674966041 KCND3 strong
RS151164490 KCND3 strong
RS1664632655 KCND3 strong
RS2101997230 KCND3 strong
RS1247179970 KCND3 strong
RS2101995228 KCND3 strong
RS778141653 KCND3 strong
RS1571939827 KCND3 strong
RS762528364 KCND3 strong
RS2101995572 KCND3 strong
RS2101995530 KCND3 strong
RS974769346 KCND3 strong
RS752589615 KCND3 strong
RS139901716 KCND3 strong
RS1167459243 KCND3 strong
RS2525053501 KCND3 strong
RS2525053579 KCND3 strong
RS2525699283 KCND3 strong
RS2525698722 KCND3 strong
RS149008060 KCND3 strong
RS397515476 KCND3 strong
RS397515478 KCND3 strong
RS150401343 KCND3 strong
RS149344567 KCND3 strong
RS786205867 KCND3 strong
RS797045634 KCND3 strong
RS142744204 KCND3 strong
RS35027371 KCND3 strong
RS201340369 KCND3 strong
RS1057519453 KCND3 strong
RS1057521793 KCND3 strong
RS397515475 KCND3 strong
RS199637120 KCND3 strong
RS376408039 KCND3 strong
RS547323858 LAMA4 strong
RS1411627342 KCND3 strong
RS778053688 KCND3 strong
RS771703569 KCND3 strong
RS771878661 KCND3 strong
RS200212002 KCND3 strong
RS186194682 KCND3 strong
RS1571636501 KCND3 strong
RS1571636508 KCND3 strong
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