SLC30A10, solute carrier family 30 member 10, 55532

N. diseases: 120; N. variants: 22
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11118406
rs11118406
Entrez Id: 55532;105372926
Gene Symbol: SLC30A10;LOC105372926
SLC30A10;LOC105372926
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease
T 0.700 GeneticVariation GWASCAT Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations. 30804561 2019
dbSNP: rs1776029
rs1776029
Entrez Id: 55532
Gene Symbol: SLC30A10
SLC30A10
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2275707
rs2275707
Entrez Id: 55532
Gene Symbol: SLC30A10
SLC30A10
CUI: C0427460
Disease:
Red cell distribution width determination
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2275707
rs2275707
Entrez Id: 55532
Gene Symbol: SLC30A10
SLC30A10
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs12024492
rs12024492
Entrez Id: 55532;105372926
Gene Symbol: SLC30A10;LOC105372926
SLC30A10;LOC105372926
CUI: C0040420
Disease:
Tonometry
C 0.700 GeneticVariation GWASCAT Genome-wide association analyses identify new loci influencing intraocular pressure. 29617998 2018
dbSNP: rs1418752
rs1418752
Entrez Id: 55532;105372926
Gene Symbol: SLC30A10;LOC105372926
SLC30A10;LOC105372926
CUI: C0040420
Disease:
Tonometry
T 0.700 GeneticVariation GWASCAT Genome-wide association analyses identify new loci influencing intraocular pressure. 29617998 2018
dbSNP: rs185048405
rs185048405
Entrez Id: 55532;105372926
Gene Symbol: SLC30A10;LOC105372926
SLC30A10;LOC105372926
CUI: C0005938
Disease:
Bone Density
T 0.700 GeneticVariation GWASCAT Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects. 29304378 2018
dbSNP: rs4846580
rs4846580
Entrez Id: 55532;105372926
Gene Symbol: SLC30A10;LOC105372926
SLC30A10;LOC105372926
CUI: C0005938
Disease:
Bone Density
A 0.700 GeneticVariation GWASCAT Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects. 29304378 2018
dbSNP: rs5781151
rs5781151
Entrez Id: 55532
Gene Symbol: SLC30A10
SLC30A10
CUI: C0206161
Disease:
Reticulocyte count (procedure)
CA 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs1057519589
rs1057519589
Entrez Id: 55532;107985281
Gene Symbol: SLC30A10;LOC107985281
SLC30A10;LOC107985281
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis
A 0.700 CausalMutation CLINVAR
dbSNP: rs1057519590
rs1057519590
Entrez Id: 55532;107985281
Gene Symbol: SLC30A10;LOC107985281
SLC30A10;LOC107985281
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis
C 0.700 CausalMutation CLINVAR
dbSNP: rs1553313783
rs1553313783
Entrez Id: 55532;107985281
Gene Symbol: SLC30A10;LOC107985281
SLC30A10;LOC107985281
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis
G 0.700 CausalMutation CLINVAR
dbSNP: rs1553313839
rs1553313839
Entrez Id: 55532;107985281
Gene Symbol: SLC30A10;LOC107985281
SLC30A10;LOC107985281
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis
G 0.700 CausalMutation CLINVAR
dbSNP: rs281860284
rs281860284
Entrez Id: 55532;107985281
Gene Symbol: SLC30A10;LOC107985281
SLC30A10;LOC107985281
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis
G 0.700 CausalMutation CLINVAR
dbSNP: rs281860285
rs281860285
Entrez Id: 55532;107985281
Gene Symbol: SLC30A10;LOC107985281
SLC30A10;LOC107985281
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis
T 0.700 CausalMutation CLINVAR
dbSNP: rs281860286
rs281860286
Entrez Id: 55532;107985281
Gene Symbol: SLC30A10;LOC107985281
SLC30A10;LOC107985281
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis
G 0.700 CausalMutation CLINVAR
dbSNP: rs281860287
rs281860287
Entrez Id: 55532;107985281
Gene Symbol: SLC30A10;LOC107985281
SLC30A10;LOC107985281
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis
G 0.700 CausalMutation CLINVAR
dbSNP: rs281860288
rs281860288
Entrez Id: 55532;107985281
Gene Symbol: SLC30A10;LOC107985281
SLC30A10;LOC107985281
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis
T 0.700 CausalMutation CLINVAR
dbSNP: rs281860289
rs281860289
Entrez Id: 55532
Gene Symbol: SLC30A10
SLC30A10
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis
G 0.700 CausalMutation CLINVAR
dbSNP: rs281860290
rs281860290
Entrez Id: 55532
Gene Symbol: SLC30A10
SLC30A10
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis
A 0.700 CausalMutation CLINVAR
dbSNP: rs281860291
rs281860291
Entrez Id: 55532
Gene Symbol: SLC30A10
SLC30A10
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis
G 0.700 CausalMutation CLINVAR
dbSNP: rs281860292
rs281860292
Entrez Id: 55532
Gene Symbol: SLC30A10
SLC30A10
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis
C 0.700 CausalMutation CLINVAR
dbSNP: rs770740586
rs770740586
Entrez Id: 55532
Gene Symbol: SLC30A10
SLC30A10
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis
A 0.700 CausalMutation CLINVAR