Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C3887485
Disease: MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1 		20 0 2 5.3E-02 0 0
CUI: C0751706
Disease: Primary Progressive Nonfluent Aphasia
Primary Progressive Nonfluent Aphasia 		21 0 2 5.1E-02 0 0
CUI: C0264097
Disease: Calcaneal apophysitis
Calcaneal apophysitis 		1 0 1 5.0E-02 0 0
CUI: C0393890
Disease: Suprascapular nerve compression
Suprascapular nerve compression 		1 0 1 5.0E-02 0 0
CUI: C0858613
Disease: Optic nerve oedema
Optic nerve oedema 		1 0 1 5.0E-02 0 0
CUI: C2675207
Disease: URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 4
URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 4 		1 0 1 5.0E-02 0 0
CUI: C3149907
Disease: AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 13
AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 13 		1 0 1 5.0E-02 0 0
CUI: C3540094
Disease: INTERLEUKIN 6, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS
INTERLEUKIN 6, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 		1 0 1 5.0E-02 0 0
CUI: C3553493
Disease: SOLUBLE INTERLEUKIN-6 RECEPTOR, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS
SOLUBLE INTERLEUKIN-6 RECEPTOR, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 		1 0 1 5.0E-02 0 0
CUI: C4049395
Disease: Chronic hepatitis C genotype 2
Chronic hepatitis C genotype 2 		1 0 1 5.0E-02 0 0
CUI: C4225298
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 104
DEAFNESS, AUTOSOMAL RECESSIVE 104 		1 0 1 5.0E-02 0 0
CUI: C4225670
Disease: ANHIDROSIS, FAMILIAL GENERALIZED, WITH ABNORMAL OR ABSENT SWEAT GLANDS
ANHIDROSIS, FAMILIAL GENERALIZED, WITH ABNORMAL OR ABSENT SWEAT GLANDS 		1 0 1 5.0E-02 0 0
CUI: C0024528
Disease: Malaise and fatigue
Malaise and fatigue 		2 0 1 4.8E-02 0 0
CUI: C0494479
Disease: Other headache syndrome
Other headache syndrome 		2 0 1 4.8E-02 0 0
CUI: C1112211
Disease: Hepatic Infection
Hepatic Infection 		24 0 2 4.8E-02 0 0
CUI: C1367972
Disease: Phlebitis and thrombophlebitis
Phlebitis and thrombophlebitis 		2 0 1 4.8E-02 0 0
CUI: C1619716
Disease: Cystatin C measurement
Cystatin C measurement 		2 0 1 4.8E-02 0 0
CUI: C1836824
Disease: Amish Infantile Epilepsy Syndrome
Amish Infantile Epilepsy Syndrome 		2 0 1 4.8E-02 0 0
CUI: C3888909
Disease: BAFF polymorphism
BAFF polymorphism 		2 0 1 4.8E-02 0 0
CUI: C4023053
Disease: Cerebellar Purkinje layer atrophy
Cerebellar Purkinje layer atrophy 		2 0 1 4.8E-02 0 0
CUI: C4024706
Disease: Spinal cord posterior columns myelin loss
Spinal cord posterior columns myelin loss 		2 0 1 4.8E-02 0 0
CUI: C4049393
Disease: Chronic hepatitis C genotype 1a
Chronic hepatitis C genotype 1a 		2 0 1 4.8E-02 0 0
CUI: C1842247
Disease: CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1 		25 35 2 4.7E-02 2 3.8E-02
CUI: C0042879
Disease: Vitamin K Assay
Vitamin K Assay 		3 6 1 4.5E-02 1 4.2E-02
CUI: C0449439
Disease: Carrier status
Carrier status 		3 0 1 4.5E-02 0 0