Muscular Dystrophy-dystroglycanopathy (congenital with Brain and Eye Anomalies)

Ophthalmic 1,016 variants 5 genes

Upload your DNA to see your personal risk score for Muscular Dystrophy-dystroglycanopathy (congenital with Brain and Eye Anomalies).

Associated Genes (5)

POMGNT1 POMT1 FKRP POMT2 FKTN

Associated Variants (1,016)

RSID	Gene	Risk Allele	Odds Ratio	Evidence
RS28942068	POMGNT1	—	—	strong
RS587777818	POMT1	—	—	strong
RS119462982	POMT1	—	—	strong
RS119462983	POMT1	—	—	strong
RS119462985	POMT1	—	—	strong
RS119462987	POMT1	—	—	strong
RS1051679985	POMT1	—	—	strong
RS587777819	POMT1	—	—	strong
RS587777820	POMT1	—	—	strong
RS398124245	POMT1	—	—	strong
RS587777821	POMGNT1	—	—	strong
RS193919335	POMGNT1	—	—	strong
RS386834017	POMGNT1	—	—	strong
RS587777817	POMT1	—	—	strong
RS28940869	POMGNT1	—	—	strong
RS193919336	POMGNT1	—	—	strong
RS193919337	POMGNT1	—	—	strong
RS587777822	POMGNT1	—	—	strong
RS267606961	POMGNT1	—	—	strong
RS74374973	POMGNT1	—	—	strong
RS267606962	POMGNT1	—	—	strong
RS386834035	POMGNT1	—	—	strong
RS267606960	POMGNT1	—	—	strong
RS104894679	FKRP	—	—	strong
RS2539378110	POMT1	—	—	strong
RS533916138	POMT2	—	—	strong
RS587777813	FKTN	—	—	strong
RS398123555	FKTN	—	—	strong
RS119463996	FKTN	—	—	strong
RS587777748	FKTN	—	—	strong
RS119463991	FKTN	—	—	strong
RS119463992	FKTN	—	—	strong
RS2539985441	FKTN	—	—	strong
RS119463995	FKTN	—	—	strong
RS119464997	FKTN	—	—	strong
RS119464998	FKTN	—	—	strong
RS267606814	FKTN	—	—	strong
RS119463989	POMT2	—	—	strong
RS119463990	FKTN	—	—	strong
RS587777815	POMT2	—	—	strong
RS200198778	POMT2	—	—	strong
RS267606969	POMT2	—	—	strong
RS267606964	POMT2	—	—	strong
RS190285831	POMT2	—	—	strong
RS267606965	POMT2	—	—	strong
RS267606971	POMT2	—	—	strong
RS267606970	POMT2	—	—	strong
RS587777816	POMT2	—	—	strong
RS918556979	POMT2	—	—	strong
RS119462981	POMT1	—	—	strong

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