FIGNL1, fidgetin like 1, 63979

N. diseases: 23; N. variants: 60
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137853208
rs137853208
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1291564
Disease:
Deficiency of aromatic-L-amino-acid decarboxylase 		0.800 GeneticVariation UNIPROT Levodopa-responsive aromatic L-amino acid decarboxylase deficiency. 14991824 2004
dbSNP: rs137853208
rs137853208
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1291564
Disease:
Deficiency of aromatic-L-amino-acid decarboxylase 		A 0.800 CausalMutation CLINVAR
dbSNP: rs137853208
rs137853208
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1291564
Disease:
Deficiency of aromatic-L-amino-acid decarboxylase 		0.800 GeneticVariation UNIPROT Aromatic L-amino acid decarboxylase deficiency: clinical features, treatment, and prognosis. 15079002 2004
dbSNP: rs137853209
rs137853209
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1291564
Disease:
Deficiency of aromatic-L-amino-acid decarboxylase 		0.800 GeneticVariation UNIPROT Levodopa-responsive aromatic L-amino acid decarboxylase deficiency. 14991824 2004
dbSNP: rs137853209
rs137853209
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1291564
Disease:
Deficiency of aromatic-L-amino-acid decarboxylase 		G 0.800 CausalMutation CLINVAR
dbSNP: rs137853209
rs137853209
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1291564
Disease:
Deficiency of aromatic-L-amino-acid decarboxylase 		0.800 GeneticVariation UNIPROT Aromatic L-amino acid decarboxylase deficiency: clinical features, treatment, and prognosis. 15079002 2004
dbSNP: rs137853210
rs137853210
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1291564
Disease:
Deficiency of aromatic-L-amino-acid decarboxylase 		0.800 GeneticVariation UNIPROT Aromatic L-amino acid decarboxylase deficiency: clinical features, treatment, and prognosis. 15079002 2004
dbSNP: rs137853210
rs137853210
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1291564
Disease:
Deficiency of aromatic-L-amino-acid decarboxylase 		0.800 GeneticVariation UNIPROT Levodopa-responsive aromatic L-amino acid decarboxylase deficiency. 14991824 2004
dbSNP: rs137853210
rs137853210
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1291564
Disease:
Deficiency of aromatic-L-amino-acid decarboxylase 		G 0.800 CausalMutation CLINVAR
dbSNP: rs137853212
rs137853212
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1291564
Disease:
Deficiency of aromatic-L-amino-acid decarboxylase 		0.800 GeneticVariation UNIPROT Aromatic L-amino acid decarboxylase deficiency: clinical features, treatment, and prognosis. 15079002 2004
dbSNP: rs137853212
rs137853212
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1291564
Disease:
Deficiency of aromatic-L-amino-acid decarboxylase 		T 0.800 CausalMutation CLINVAR
dbSNP: rs137853212
rs137853212
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1291564
Disease:
Deficiency of aromatic-L-amino-acid decarboxylase 		0.800 GeneticVariation UNIPROT Levodopa-responsive aromatic L-amino acid decarboxylase deficiency. 14991824 2004
dbSNP: rs201951824
rs201951824
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1291564
Disease:
Deficiency of aromatic-L-amino-acid decarboxylase 		T 0.800 CausalMutation CLINVAR Aromatic L-amino acid decarboxylase deficiency: clinical features, treatment, and prognosis. 15079002 2004
dbSNP: rs201951824
rs201951824
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1291564
Disease:
Deficiency of aromatic-L-amino-acid decarboxylase 		0.800 GeneticVariation UNIPROT Levodopa-responsive aromatic L-amino acid decarboxylase deficiency. 14991824 2004
dbSNP: rs201951824
rs201951824
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1291564
Disease:
Deficiency of aromatic-L-amino-acid decarboxylase 		T 0.800 CausalMutation CLINVAR Aromatic L-amino acid decarboxylase enzyme activity in deficient patients and heterozygotes. 17240182 2007
dbSNP: rs201951824
rs201951824
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1291564
Disease:
Deficiency of aromatic-L-amino-acid decarboxylase 		0.800 GeneticVariation UNIPROT Aromatic L-amino acid decarboxylase deficiency: clinical features, treatment, and prognosis. 15079002 2004
dbSNP: rs201951824
rs201951824
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1291564
Disease:
Deficiency of aromatic-L-amino-acid decarboxylase 		T 0.800 CausalMutation CLINVAR Clinical and biochemical features of aromatic L-amino acid decarboxylase deficiency. 20505134 2010
dbSNP: rs2167364
rs2167364
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1961102
Disease:
Precursor Cell Lymphoblastic Leukemia Lymphoma 		G 0.800 GeneticVariation GWASCAT Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia. 22076464 2012
dbSNP: rs2167364
rs2167364
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1961102
Disease:
Precursor Cell Lymphoblastic Leukemia Lymphoma 		C 0.800 GeneticVariation GWASDB Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. 23512250 2013
dbSNP: rs1037351
rs1037351
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1961102
Disease:
Precursor Cell Lymphoblastic Leukemia Lymphoma 		C 0.700 GeneticVariation GWASDB Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. 23512250 2013
dbSNP: rs10899734
rs10899734
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs10899735
rs10899735
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs10899736
rs10899736
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1961102
Disease:
Precursor Cell Lymphoblastic Leukemia Lymphoma 		C 0.700 GeneticVariation GWASDB Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. 23512250 2013
dbSNP: rs11238138
rs11238138
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs11575387
rs11575387
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1961102
Disease:
Precursor Cell Lymphoblastic Leukemia Lymphoma 		C 0.700 GeneticVariation GWASDB Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. 23512250 2013