Hereditary Ataxia

Other 33 variants 26 genes

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Associated Genes (26)

PRKCG MFN2 ATP1A3 KIF11 KIF1A SYNE1 KCND3 PKD1 SYNGAP1 LITAF CAMK2B NKX2-1 CLCN2 ADCY5 ARID1B EYA1 ALG13 APTX POLR3A MFSD8 SACS WFS1 SPG7 SCN9A L1CAM KCNC3

Associated Variants (33)

RSID	Gene	Risk Allele	Odds Ratio	Evidence
RS1486368788	PRKCG	—	—	strong
RS376598131	MFN2	—	—	strong
RS1599725621	ATP1A3	—	—	strong
RS201865099	KIF11	—	—	strong
RS368124753	KIF1A	—	—	strong
RS760076679	SYNE1	—	—	strong
RS1664632655	KCND3	—	—	strong
RS201991587	PKD1	—	—	strong
RS1405483444	SYNGAP1	—	—	strong
RS375665454	LITAF	—	—	strong
RS555460132	CAMK2B	—	—	strong
RS760880632	NKX2-1	—	—	strong
RS377119457	CLCN2	—	—	strong
RS373748121	ADCY5	—	—	strong
RS890215101	ARID1B	—	—	strong
RS2537297433	EYA1	—	—	strong
RS778296473	ALG13	—	—	strong
RS104894103	APTX	—	—	strong
RS774007232	POLR3A	—	—	strong
RS868732642	MFSD8	—	—	strong
RS1555252349	SACS	—	—	strong
RS374128662	SACS	—	—	strong
RS867249938	SACS	—	—	strong
RS191875469	POLR3A	—	—	strong
RS183359489	KIF1A	—	—	strong
RS147147660	WFS1	—	—	strong
RS117461489	SYNE1	—	—	strong
RS369227537	SPG7	—	—	strong
RS141268327	SCN9A	—	—	strong
RS36021462	L1CAM	—	—	strong
RS61755320	SPG7	—	—	strong
RS104894699	KCNC3	—	—	strong
RS121918358	SPG7	—	—	strong