With Oculomotor Apraxia and Hypoalbuminemia

Other 36 variants 3 genes

Upload your DNA to see your personal risk score for With Oculomotor Apraxia and Hypoalbuminemia.

Associated Genes (3)

APTX SETX PNKP

Associated Variants (36)

RSID	Gene	Risk Allele	Odds Ratio	Evidence
RS1015321377	APTX	—	—	strong
RS1554664711	APTX	—	—	strong
RS140355580	APTX	—	—	strong
RS371868908	APTX	—	—	strong
RS1563963464	APTX	—	—	strong
RS1563945076	APTX	—	—	strong
RS751250105	APTX	—	—	strong
RS146487634	APTX	—	—	strong
RS1828552847	APTX	—	—	strong
RS111392103	APTX	—	—	strong
RS1847100683	SETX	—	—	strong
RS748165574	APTX	—	—	strong
RS2118688818	APTX	—	—	strong
RS770007531	APTX	—	—	strong
RS1225927323	APTX	—	—	strong
RS2118686800	APTX	—	—	strong
RS2489453836	APTX	—	—	strong
RS2489448115	APTX	—	—	strong
RS587784366	PNKP	—	—	strong
RS121908131	APTX	—	—	strong
RS587776594	APTX	—	—	strong
RS121908132	APTX	—	—	strong
RS121908133	APTX	—	—	strong
RS1587330671	APTX	—	—	strong
RS104894103	APTX	—	—	strong
RS267606665	APTX	—	—	strong
RS141493373	APTX	—	—	strong
RS587776593	APTX	—	—	strong
RS141195622	APTX	—	—	strong
RS144076460	APTX	—	—	strong
RS140888559	APTX	—	—	strong
RS113391831	APTX	—	—	strong
RS201736194	APTX	—	—	strong
RS201912053	APTX	—	—	strong
RS1114167423	APTX	—	—	strong
RS904293109	APTX	—	—	strong