fitSNPs 
Functionally Interploating SNPs
AILUN | GENE CHAnge browSER
     
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DisorderLociGeneDescriptionDER
Holoprosencephaly-1 (2)21q22.3RUNX1runt-related transcription factor 1 (acute myeloid leukemia 1; aml1 oncogene)0.717
Tukel syndrome (2)21q22RUNX1runt-related transcription factor 1 (acute myeloid leukemia 1; aml1 oncogene)0.717
"Dermatitis, atopic, 603165 (2)"5q31-q33CTNNA1"catenin (cadherin-associated protein), alpha 1, 102kDa"0.713
"Eosinophilia, familial (2)"5q31-q33CTNNA1"catenin (cadherin-associated protein), alpha 1, 102kDa"0.713
"Glaucoma 1, open angle, M (2)"5q22.1-q32CTNNA1"catenin (cadherin-associated protein), alpha 1, 102kDa"0.713
"Hemangioma, capillary infantile (2)"5q31-q33CTNNA1"catenin (cadherin-associated protein), alpha 1, 102kDa"0.713
"Paget disease of bone, 602080 (2)"5q31CTNNA1"catenin (cadherin-associated protein), alpha 1, 102kDa"0.713
"{Autoimmune thyroid disease, susceptibility to, 2} (2)"5q31-q33CTNNA1"catenin (cadherin-associated protein), alpha 1, 102kDa"0.713
"{Celiac disease, susceptibility to, 2} (2)"5q31-q33CTNNA1"catenin (cadherin-associated protein), alpha 1, 102kDa"0.713
"{Diabetes mellitus, insulin-dependent, 18} (2)"5q31.1-q33.1CTNNA1"catenin (cadherin-associated protein), alpha 1, 102kDa"0.713
"{Inflammatory bowel disease-5}, 266600 (2)"5q31CTNNA1"catenin (cadherin-associated protein), alpha 1, 102kDa"0.713
"{Malaria, intensity of infection} (2)"5q31-q33CTNNA1"catenin (cadherin-associated protein), alpha 1, 102kDa"0.713
"{Schistosoma mansoni infection, susceptibility/resistance to} (2)"5q31-q33CTNNA1"catenin (cadherin-associated protein), alpha 1, 102kDa"0.713
{?Allergy and asthma susceptibility} (2)5q31.1CTNNA1"catenin (cadherin-associated protein), alpha 1, 102kDa"0.713
"{Autism, susceptibility to, 6} (2)"17q11NF1"neurofibromin 1 (neurofibromatosis, von Recklinghausen disease, Watson disease)"0.713
"Pseudohyperkalemia, familial, 2, due to red cell leak (2)"2q35-q36OBSL1obscurin-like 10.713
"Syndactyly, type 1 (2)"2q34-q36OBSL1obscurin-like 10.713
"{Systemic lupus erythematosus with nephritis, susceptibility to, 2} (2)"2q34-q35OBSL1obscurin-like 10.713
"{Tuberculosis, susceptibility to} (2)"2q35OBSL1obscurin-like 10.713
"Atrial septal defect, secundum type (2)"6p21.3HLA-DQA2"major histocompatibility complex, class II, DQ alpha 2"0.706
"Deafness, autosomal recessive 66 (2)"6p22.3-p21.2HLA-DQA2"major histocompatibility complex, class II, DQ alpha 2"0.706
"Epilepsy, juvenile myoclonic 3 (2)"6p21HLA-DQA2"major histocompatibility complex, class II, DQ alpha 2"0.706
"Panbronchiolitis, diffuse (2)"6p21.3HLA-DQA2"major histocompatibility complex, class II, DQ alpha 2"0.706
"Spinocerebellar ataxia, autosomal recessive 3 (2)"6p23-p21HLA-DQA2"major histocompatibility complex, class II, DQ alpha 2"0.706
"{Azoospremia, nonobstructive} (2)"6p21.3HLA-DQA2"major histocompatibility complex, class II, DQ alpha 2"0.706
"{Cataract, age-related cortical, susceptibility to} (2)"6p12-q12HLA-DQA2"major histocompatibility complex, class II, DQ alpha 2"0.706
"{Diabetes mellitus, insulin-dependent-1} (2)"6p21.3HLA-DQA2"major histocompatibility complex, class II, DQ alpha 2"0.706
"{Macroglobulinemia, Waldenstrom, susceptibility to, 1} (2)"6p21.3HLA-DQA2"major histocompatibility complex, class II, DQ alpha 2"0.706
Immunoglobulin A deficiency (2)6p21.3HLA-DQA2"major histocompatibility complex, class II, DQ alpha 2"0.706
Laryngeal adductor paralysis (2) (?)6p21.3-p21.2HLA-DQA2"major histocompatibility complex, class II, DQ alpha 2"0.706
Myasthenia gravis with thymus hyperplasia (2)6p21.3HLA-DQA2"major histocompatibility complex, class II, DQ alpha 2"0.706
Otosclerosis 3 (2)6p22.3-p21.3HLA-DQA2"major histocompatibility complex, class II, DQ alpha 2"0.706
Wegener granulomatosis (2)6p21.3HLA-DQA2"major histocompatibility complex, class II, DQ alpha 2"0.706
"Ataxia, sensory, autosomal dominant (2)"8p12-q12.1RAB2A"RAB2A, member RAS oncogene family"0.704
"Dystonia-6, torsion (2)"8p21-q22RAB2A"RAB2A, member RAS oncogene family"0.704
"Preauricular fistulae, congenital (2) (?)"8q11.1-q13.3RAB2A"RAB2A, member RAS oncogene family"0.704
"{Mycobacterium tuberculosis, susceptibility to, 2} (2)"8q12-q13RAB2A"RAB2A, member RAS oncogene family"0.704
Spastic paraplegia-5A (2)8p12-q13RAB2A"RAB2A, member RAS oncogene family"0.704
{Alzheimer disease 12} (2)8p12-q22RAB2A"RAB2A, member RAS oncogene family"0.704
"Aortic aneurysm, familial thoracic 2 (2)"5q13-q14SERINC5serine incorporator 50.703
"Capillary malformations, hereditary (2)"5q13-q22SERINC5serine incorporator 50.703
"Fibromatosis, gingival, 2, 135300 (2)"5q13-q22SERINC5serine incorporator 50.703
"Myoclonic epilepsy, juvenile, 4 (2)"5q12-q14SERINC5serine incorporator 50.703
"Striatal degeneration, autosomal dominant (2)"5q13.3-q14.1SERINC5serine incorporator 50.703
"Epilepsy, myoclonic, benign adult familial, type 2 (2)"2p11.1-q12.2TGOLN2trans-golgi network protein 20.702
Retinitis pigmentosa-28 (2)2p15-p11TGOLN2trans-golgi network protein 20.702
"Aneurysm, intracranial berry, 5 (2)"2p15-q14SPTBN1"spectrin, beta, non-erythrocytic 1"0.701
"Epilepsy, myoclonic, benign adult familial, type 2 (2)"2p11.1-q12.2SPTBN1"spectrin, beta, non-erythrocytic 1"0.701
Spinocerebellar ataxia 25 (3)2p21-p13SPTBN1"spectrin, beta, non-erythrocytic 1"0.701
"Opitz G syndrome, type II (2)"22q11.2IGL@immunoglobulin lambda locus0.696