Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs441460
rs441460
Entrez Id: 55604
Gene Symbol: CARMIL1
CARMIL1
CUI: C0032181
Disease:
Platelet Count measurement 		G 0.800 GeneticVariation GWASCAT New gene functions in megakaryopoiesis and platelet formation. 22139419 2011
dbSNP: rs441460
rs441460
Entrez Id: 55604
Gene Symbol: CARMIL1
CARMIL1
CUI: C0032181
Disease:
Platelet Count measurement 		G 0.800 GeneticVariation GWASDB New gene functions in megakaryopoiesis and platelet formation. 22139419 2011
dbSNP: rs742132
rs742132
Entrez Id: 55604
Gene Symbol: CARMIL1
CARMIL1
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		A 0.800 GeneticVariation GWASDB Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations. 19503597 2009
dbSNP: rs742132
rs742132
Entrez Id: 55604
Gene Symbol: CARMIL1
CARMIL1
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		A 0.800 GeneticVariation GWASCAT Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations. 19503597 2009
dbSNP: rs116272812
rs116272812
Entrez Id: 55604
Gene Symbol: CARMIL1
CARMIL1
CUI: C0427460
Disease:
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs116272812
rs116272812
Entrez Id: 55604
Gene Symbol: CARMIL1
CARMIL1
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs116272812
rs116272812
Entrez Id: 55604
Gene Symbol: CARMIL1
CARMIL1
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: rs116418977
rs116418977
Entrez Id: 8418;55604
Gene Symbol: CMAHP;CARMIL1
CMAHP;CARMIL1
CUI: C0021704
Disease:
Intelligence 		T 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs2328887
rs2328887
Entrez Id: 8418;55604
Gene Symbol: CMAHP;CARMIL1
CMAHP;CARMIL1
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs35789010
rs35789010
Entrez Id: 55604
Gene Symbol: CARMIL1
CARMIL1
CUI: C0011849
Disease:
Diabetes Mellitus 		A 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708 2019
dbSNP: rs35789010
rs35789010
Entrez Id: 55604
Gene Symbol: CARMIL1
CARMIL1
CUI: C0017654
Disease:
Glomerular Filtration Rate 		A 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708 2019
dbSNP: rs35789010
rs35789010
Entrez Id: 55604
Gene Symbol: CARMIL1
CARMIL1
CUI: C0011847
Disease:
Diabetes 		A 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708 2019
dbSNP: rs35789010
rs35789010
Entrez Id: 55604
Gene Symbol: CARMIL1
CARMIL1
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs62392365
rs62392365
Entrez Id: 8418;55604
Gene Symbol: CMAHP;CARMIL1
CMAHP;CARMIL1
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs6918354
rs6918354
Entrez Id: 8418;55604
Gene Symbol: CMAHP;CARMIL1
CMAHP;CARMIL1
CUI: C0036341
Disease:
Schizophrenia 		T 0.700 GeneticVariation GWASCAT Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect. 30285260 2019
dbSNP: rs7774567
rs7774567
Entrez Id: 8418;55604
Gene Symbol: CMAHP;CARMIL1
CMAHP;CARMIL1
CUI: C0036341
Disease:
Schizophrenia 		0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. 31374203 2019
dbSNP: rs7774567
rs7774567
Entrez Id: 8418;55604
Gene Symbol: CMAHP;CARMIL1
CMAHP;CARMIL1
CUI: C0021704
Disease:
Intelligence 		0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. 31374203 2019
dbSNP: rs13212936
rs13212936
Entrez Id: 55604
Gene Symbol: CARMIL1
CARMIL1
CUI: C0021704
Disease:
Intelligence 		0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs34991172
rs34991172
Entrez Id: 55604
Gene Symbol: CARMIL1
CARMIL1
CUI: C0021704
Disease:
Intelligence 		0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs62392365
rs62392365
Entrez Id: 8418;55604
Gene Symbol: CMAHP;CARMIL1
CMAHP;CARMIL1
CUI: C0021704
Disease:
Intelligence 		0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs75063949
rs75063949
Entrez Id: 55604
Gene Symbol: CARMIL1
CARMIL1
CUI: C0003125
Disease:
Anorexia Nervosa 		0.700 GeneticVariation GWASCAT Examination of the shared genetic basis of anorexia nervosa and obsessive-compulsive disorder. 30087453 2018
dbSNP: rs75063949
rs75063949
Entrez Id: 55604
Gene Symbol: CARMIL1
CARMIL1
CUI: C0028768
Disease:
Obsessive-Compulsive Disorder 		0.700 GeneticVariation GWASCAT Examination of the shared genetic basis of anorexia nervosa and obsessive-compulsive disorder. 30087453 2018
dbSNP: rs111722075
rs111722075
Entrez Id: 8418;55604
Gene Symbol: CMAHP;CARMIL1
CMAHP;CARMIL1
CUI: C1318312
Disease:
Serum iron measurement 		C 0.700 GeneticVariation GWASCAT Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation? 28334935 2017
dbSNP: rs111722075
rs111722075
Entrez Id: 8418;55604
Gene Symbol: CMAHP;CARMIL1
CMAHP;CARMIL1
CUI: C1277709
Disease:
Transferrin saturation measurement 		C 0.700 GeneticVariation GWASCAT Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation? 28334935 2017
dbSNP: rs183360145
rs183360145
Entrez Id: 8418;55604
Gene Symbol: CMAHP;CARMIL1
CMAHP;CARMIL1
CUI: C1283048
Disease:
Iron binding capacity total measurement 		T 0.700 GeneticVariation GWASCAT Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation? 28334935 2017