Joubert Syndrome and Related Disorders

Other 189 variants 15 genes

Upload your DNA to see your personal risk score for Joubert Syndrome and Related Disorders.

Associated Genes (15)

AHI1 KIAA0586 RPGRIP1L INPP5E TCTN2 CC2D2A CPLANE1 TMEM67 TMEM231 ARL13B NPHP3 B9D2 TMEM237 TMEM138 TCTN3

Associated Variants (189)

RSID	Gene	Risk Allele	Odds Ratio	Evidence
RS863225131	AHI1	—	—	strong
RS534542684	KIAA0586	—	—	strong
RS757350052	KIAA0586	—	—	strong
RS797045104	RPGRIP1L	—	—	strong
RS199873582	INPP5E	—	—	strong
RS760830696	TCTN2	—	—	strong
RS201502401	CC2D2A	—	—	strong
RS863225175	CC2D2A	—	—	strong
RS374144275	CPLANE1	—	—	strong
RS775263897	CPLANE1	—	—	strong
RS749523755	CPLANE1	—	—	strong
RS530569572	CPLANE1	—	—	strong
RS756856188	CPLANE1	—	—	strong
RS777686211	CPLANE1	—	—	strong
RS371637724	AHI1	—	—	strong
RS777668842	AHI1	—	—	strong
RS863225143	AHI1	—	—	strong
RS753874898	AHI1	—	—	strong
RS863225142	AHI1	—	—	strong
RS863225138	AHI1	—	—	strong
RS750950408	TMEM67	—	—	strong
RS863225238	TMEM67	—	—	strong
RS863225240	TMEM67	—	—	strong
RS863225200	INPP5E	—	—	strong
RS770748954	TMEM231	—	—	strong
RS374349989	TCTN2	—	—	strong
RS121918130	INPP5E	—	—	strong
RS121918198	RPGRIP1L	—	—	strong
RS121918199	RPGRIP1L	—	—	strong
RS137853107	TMEM67	—	—	strong
RS199821258	TMEM67	—	—	strong
RS137853108	TMEM67	—	—	strong
RS267607119	TMEM67	—	—	strong
RS201893408	TMEM67	—	—	strong
RS202149403	TMEM67	—	—	strong
RS121912608	ARL13B	—	—	strong
RS267606916	NPHP3	—	—	strong
RS1487082103	B9D2	—	—	strong
RS121918128	INPP5E	—	—	strong
RS199469707	TMEM237	—	—	strong
RS917404097	TMEM138	—	—	strong
RS387907135	TMEM138	—	—	strong
RS367543061	CPLANE1	—	—	strong
RS367543062	CPLANE1	—	—	strong
RS793888508	TCTN3	—	—	strong
RS397514609	TMEM231	—	—	strong
RS200799769	TMEM231	—	—	strong
RS386834182	TMEM67	—	—	strong
RS386834202	TMEM67	—	—	strong
RS398124546	NPHP3	—	—	strong

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