Inborn Genetic Diseases

Other 33,494 variants 23 genes

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Associated Genes (23)

WFS1 covers 10 genes, none of which curated to show dosage sensitivity DPYD HADH CACNA1S GCK AGL DARS2 INF2 SPG11 FHOD3 PAH TMEM216 AGA VWF INPP5E DUOXA2 ALDOB HFE FBP1 GLB1 OCA2 LCA5

Associated Variants (33,494)

RSID	Gene	Risk Allele	Odds Ratio	Evidence
RS1553878931	WFS1	—	—	exploratory
RS3064744	covers 10 genes, none of which curated to show dosage sensitivity	—	—	exploratory
RS67376798	DPYD	—	—	exploratory
RS55886062	DPYD	—	—	exploratory
RS202195756	WFS1	—	—	exploratory
RS727503747	WFS1	—	—	exploratory
RS766169444	WFS1	—	—	exploratory
RS56005131	DPYD	—	—	exploratory
RS376876153	HADH	—	—	exploratory
RS146418094	WFS1	—	—	exploratory
RS756869880	WFS1	—	—	exploratory
RS772226819	CACNA1S	—	—	exploratory
RS529580583	WFS1	—	—	exploratory
RS760226129	WFS1	—	—	exploratory
RS914996283	WFS1	—	—	exploratory
RS577954688	HADH	—	—	exploratory
RS150766162	HADH	—	—	exploratory
RS140773453	WFS1	—	—	exploratory
RS1182603872	GCK	—	—	exploratory
RS148994843	DPYD	—	—	exploratory
RS387906244	AGL	—	—	strong
RS142433332	DARS2	—	—	strong
RS267607183	INF2	—	—	strong
RS118203963	SPG11	—	—	strong
RS546991789	FHOD3	—	—	strong
RS62642926	PAH	—	—	strong
RS201108965	TMEM216	—	—	strong
RS386833436	AGA	—	—	strong
RS61750117	VWF	—	—	strong
RS1800386	VWF	—	—	strong
RS121918130	INPP5E	—	—	strong
RS3918290	DPYD	—	—	strong
RS4774518	DUOXA2	—	—	strong
RS1800546	ALDOB	—	—	strong
RS5030858	PAH	—	—	strong
RS62508698	PAH	—	—	strong
RS62516151	PAH	—	—	strong
RS62508588	PAH	—	—	strong
RS1800562	HFE	—	—	strong
RS5030855	PAH	—	—	strong
RS5030841	PAH	—	—	strong
RS62642937	PAH	—	—	strong
RS74603784	PAH	—	—	strong
RS76212747	PAH	—	—	strong
RS757653154	FBP1	—	—	strong
RS72555393	GLB1	—	—	strong
RS72555366	GLB1	—	—	strong
RS72555392	GLB1	—	—	strong
RS121918166	OCA2	—	—	strong
RS121918165	LCA5	—	—	strong

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