rs1064795559, MORC2

N. diseases: 29
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Clinodactyly of the 5th finger
CUI: C1850049
Disease: Clinodactyly of the 5th finger
0.700 GeneticVariation CLINVAR
Easy fatigability
CUI: C1837098
Disease: Easy fatigability
0.700 GeneticVariation CLINVAR
Hyperextensibility at elbow
CUI: C4023808
Disease: Hyperextensibility at elbow
0.700 GeneticVariation CLINVAR
Focal T2 hyperintense brainstem lesion
CUI: C4022748
Disease: Focal T2 hyperintense brainstem lesion
0.700 GeneticVariation CLINVAR
Hyperacusis
CUI: C0034880
Disease: Hyperacusis
0.700 GeneticVariation CLINVAR
Hyperextensibility of the knee
CUI: C4023802
Disease: Hyperextensibility of the knee
0.700 GeneticVariation CLINVAR
Focal T2 hyperintense basal ganglia lesion
CUI: C4024926
Disease: Focal T2 hyperintense basal ganglia lesion
0.700 GeneticVariation CLINVAR
Muscle Weakness
CUI: C0151786
Disease: Muscle Weakness
0.700 GeneticVariation CLINVAR
Broad hallux
CUI: C1867131
Disease: Broad hallux
0.700 GeneticVariation CLINVAR
Tremor of hands
CUI: C0239842
Disease: Tremor of hands
0.700 GeneticVariation CLINVAR
Hyperplasia of midface
CUI: C0240309
Disease: Hyperplasia of midface
0.700 GeneticVariation CLINVAR
Global developmental delay
CUI: C0557874
Disease: Global developmental delay
0.700 GeneticVariation CLINVAR
Soft, doughy skin
CUI: C1849043
Disease: Soft, doughy skin
0.700 GeneticVariation CLINVAR
Nevus flammeus nuchae
CUI: C4024829
Disease: Nevus flammeus nuchae
0.700 GeneticVariation CLINVAR
Congenital pectus excavatum
CUI: C0016842
Disease: Congenital pectus excavatum
0.700 GeneticVariation CLINVAR
Oral aversion
CUI: C3665983
Disease: Oral aversion
0.700 GeneticVariation CLINVAR
Focal T2 hyperintense thalamic lesion
CUI: C4022774
Disease: Focal T2 hyperintense thalamic lesion
0.700 GeneticVariation CLINVAR
Intolerant of heat
CUI: C0231274
Disease: Intolerant of heat
0.700 GeneticVariation CLINVAR
Chronic constipation
CUI: C0401149
Disease: Chronic constipation
0.700 GeneticVariation CLINVAR
Glabellar hemangioma
CUI: C1854408
Disease: Glabellar hemangioma
0.700 GeneticVariation CLINVAR
Exophoria
CUI: C0152217
Disease: Exophoria
0.700 GeneticVariation CLINVAR
Abnormal hypothalamus physiology
CUI: C4022968
Disease: Abnormal hypothalamus physiology
0.700 GeneticVariation CLINVAR
Unable to concentrate
CUI: C0235198
Disease: Unable to concentrate
0.700 GeneticVariation CLINVAR
Exercise-induced muscle fatigue
CUI: C1855580
Disease: Exercise-induced muscle fatigue
0.700 GeneticVariation CLINVAR
Prominent ear helix
CUI: C4024165
Disease: Prominent ear helix
0.700 GeneticVariation CLINVAR