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: rs4947584
rs4947584
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1305855
Disease:
Body mass index 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
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: 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: 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
dbSNP: rs11575575
rs11575575
Entrez Id: 63979
Gene Symbol: FIGNL1
FIGNL1
CUI: C1961102
Disease:
Precursor Cell Lymphoblastic Leukemia Lymphoma 		T 0.700 GeneticVariation GWASDB Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. 23512250 2013
dbSNP: rs17133853
rs17133853
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1961102
Disease:
Precursor Cell Lymphoblastic Leukemia Lymphoma 		G 0.700 GeneticVariation GWASDB Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. 23512250 2013
dbSNP: rs17152020
rs17152020
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1961102
Disease:
Precursor Cell Lymphoblastic Leukemia Lymphoma 		A 0.700 GeneticVariation GWASDB Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. 23512250 2013
dbSNP: rs3823674
rs3823674
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: rs3887825
rs3887825
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1961102
Disease:
Precursor Cell Lymphoblastic Leukemia Lymphoma 		A 0.700 GeneticVariation GWASDB Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. 23512250 2013
dbSNP: rs4947582
rs4947582
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: rs4947584
rs4947584
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1961102
Disease:
Precursor Cell Lymphoblastic Leukemia Lymphoma 		A 0.700 GeneticVariation GWASDB Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. 23512250 2013
dbSNP: rs6951648
rs6951648
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1961102
Disease:
Precursor Cell Lymphoblastic Leukemia Lymphoma 		A 0.700 GeneticVariation GWASDB Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. 23512250 2013
dbSNP: rs7791875
rs7791875
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1961102
Disease:
Precursor Cell Lymphoblastic Leukemia Lymphoma 		T 0.700 GeneticVariation GWASDB Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. 23512250 2013
dbSNP: rs7803247
rs7803247
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1961102
Disease:
Precursor Cell Lymphoblastic Leukemia Lymphoma 		T 0.700 GeneticVariation GWASDB Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. 23512250 2013
dbSNP: rs7808025
rs7808025
Entrez Id: 1644;63979
Gene Symbol: DDC;FIGNL1
DDC;FIGNL1
CUI: C1961102
Disease:
Precursor Cell Lymphoblastic Leukemia Lymphoma 		A 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: 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: rs11575457
rs11575457
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: rs11980368
rs11980368
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: rs12718528
rs12718528
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: rs12718529
rs12718529
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: rs13311361
rs13311361
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: rs1349492
rs1349492
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: rs1451372
rs1451372
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