fitSNPs 
Functionally Interploating SNPs
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GeneDERDescriptionDiseaseGAD
IDS0.739iduronate 2-sulfatase (Hunter syndrome)Mucopolysaccharidosis II / Mucopolysaccharidosis II ? / Mucopolysaccharidosis II, with seizures 
RUNX10.717runt-related transcription factor 1 (acute myeloid leukemia 1; aml1 oncogene)Platelet disorder, familial / Rheumatoid arthritis, susceptibility, association / Thrombocytopaenia,myeloblastic leukemias,asthm142251
TRA@0.715T cell receptor alpha locusIgA nephropathy141839
CTNNA10.713catenin (cadherin-associated protein), alpha 1, 102kDa  
NF10.713neurofibromin 1 (neurofibromatosis, von Recklinghausen disease, Watson disease)Neurofibromatosis 1 / Neurofibromatosis, spinal / Neurofibromatosis-Noonan syndrome / Pheochromacytoma,autism,neurofibromatosis 131555
OBSL10.713obscurin-like 1  
HLA-DQA20.706major histocompatibility complex, class II, DQ alpha 2  
SMAD30.705SMAD family member 3Osteoarthritis,bacteremia153883
RAB2A0.704RAB2A, member RAS oncogene family  
CALM10.703calmodulin 1 (phosphorylase kinase, delta)Osteoarthritis, association with,osteoarthritis138642
SERINC50.703serine incorporator 5  
TGOLN20.702trans-golgi network protein 2  
EPOR0.701erythropoietin receptorErythrocytosis / Polycythaemia / Polycythaemia?,Familial erythrocytosis122245
SPTBN10.701spectrin, beta, non-erythrocytic 1  
C8ORFK290.7hypothetical LOC340393  
IL80.698interleukin 8Gastric diseases, susept. , assoc. with / Increased transcription, association with,stomach cancer,prostate cancer,H. pylori inf128594
QKI0.698quaking homolog, KH domain RNA binding (mouse)  
IGL@0.696immunoglobulin lambda locus  
WSB10.696WD repeat and SOCS box-containing 1  
HLA-C0.695major histocompatibility complex, class I, CHLA-C null allele,psoriasis,diabetes, type 1,periodontitis,endometriosis,psoriatic arthritis,Lupus,vitiligo139623
PTGER30.695prostaglandin E receptor 3 (subtype EP3)asthma asthma, aspirin-intolerant152925
KPNB10.693karyopherin (importin) beta 1  
HNRPDL0.692heterogeneous nuclear ribonucleoprotein D-like  
GNAS0.691GNAS complex locusAlbright hereditary osteodystrophy / Albright hereditary osteodystrophy & pseudohypopar / Albright hereditary osteodystrophy, as139581
MAP2K50.691mitogen-activated protein kinase kinase 5  
ILF30.69interleukin enhancer binding factor 3, 90kDa  
ITGB10.689integrin, beta 1 (fibronectin receptor, beta polypeptide, antigen CD29 includes MDF2, MSK12)  
CALD10.688caldesmon 1nephropathy in other diseases,diabetes, type 1118067
PRDM20.688PR domain containing 2, with ZNF domainBone mineral density, association with 
CD590.687CD59 molecule, complement regulatory proteinCD59 deficiency 
CSNK1A10.686casein kinase 1, alpha 1  
GLS0.686glutaminase  
PRKCA0.686protein kinase C, alphamultiple sclerosis133139
TARP0.686TCR gamma alternate reading frame protein  
AK20.685adenylate kinase 2  
DIMT1L0.685DIM1 dimethyladenosine transferase 1-like (S. cerevisiae)  
COL6A10.684collagen, type VI, alpha 1Bethlem myopathy / Ullrich congenital muscular dystrophy,skeletal hyperostosis119519
FGFR10.684fibroblast growth factor receptor 1 (fms-related tyrosine kinase 2, Pfeiffer syndrome)Hypogonadotropic hypogonadism, idiopathic / Kallmann syndrome / Non-syndromic trigonocephaly / Osteoglophonic dysplasia / Pfeiff 
GGA20.684golgi associated, gamma adaptin ear containing, ARF binding protein 2  
PRKDC0.684protein kinase, DNA-activated, catalytic polypeptideProtein kinase deficiency 
SMARCC10.684SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1  
TNFRSF250.684tumor necrosis factor receptor superfamily, member 25Rheumatoid arthritis, association with 
PDLIM50.683PDZ and LIM domain 5schizophrenia132455
UBE2S0.683ubiquitin-conjugating enzyme E2S  
THRA0.682thyroid hormone receptor, alpha (erythroblastic leukemia viral (v-erb-a) oncogene homolog, avian)thyroid cancer136247
VEGFA0.682vascular endothelial growth factor AAtherosclerosis development, association with / Decreased VEGF plasma levels, association with / Diabetic retinopathy, associati137917
CD440.681CD44 molecule (Indian blood group)CD44 variant 
HLA-DQB10.68major histocompatibility complex, class II, DQ beta 1diabetes, type 1,pancreatitis, autoimmune; pancreatitis, chronic calcifying,periodontitis,infertility, tubal factor,allergy,myas125696
LOC4403450.68hypothetical protein LOC440345  
GM2A0.679GM2 ganglioside activatorGangliosidosis GM2