Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11628273
rs11628273
FNTB ; MAX ; CHURC1-FNTB ; MIR4706
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.800 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs11628273
rs11628273
FNTB ; MAX ; CHURC1-FNTB ; MIR4706
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.800 GeneticVariation GWASDB Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010

2009
dbSNP: rs4466998
rs4466998
FNTB ; MAX ; CHURC1-FNTB
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		A 0.800 GeneticVariation GWASDB Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010

2009
dbSNP: rs4466998
rs4466998
FNTB ; MAX ; CHURC1-FNTB
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		A 0.800 GeneticVariation GWASCAT Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010

2009
dbSNP: rs7148590
rs7148590
FNTB ; MAX ; CHURC1-FNTB
CUI: C1318315
Disease: Serum zinc measurement
Serum zinc measurement 		0.800 GeneticVariation GWASDB Genome-wide association study identifies loci affecting blood copper, selenium and zinc. 23720494

2013
dbSNP: rs7148590
rs7148590
FNTB ; MAX ; CHURC1-FNTB
CUI: C1318315
Disease: Serum zinc measurement
Serum zinc measurement 		0.800 GeneticVariation GWASCAT Genome-wide association study identifies loci affecting blood copper, selenium and zinc. 23720494

2013
dbSNP: rs11620955
rs11620955
FNTB ; MAX ; CHURC1-FNTB
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517

2012
dbSNP: rs11627485
rs11627485
FNTB ; MAX ; CHURC1-FNTB
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs11627485
rs11627485
FNTB ; MAX ; CHURC1-FNTB
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs11627485
rs11627485
FNTB ; MAX ; CHURC1-FNTB
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs11627485
rs11627485
FNTB ; MAX ; CHURC1-FNTB
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs11627485
rs11627485
FNTB ; MAX ; CHURC1-FNTB
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs11627485
rs11627485
FNTB ; MAX ; CHURC1-FNTB
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs11627531
rs11627531
FNTB ; MAX ; CHURC1-FNTB
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517

2012
dbSNP: rs11627531
rs11627531
FNTB ; MAX ; CHURC1-FNTB
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASDB Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010

2009
dbSNP: rs11628273
rs11628273
FNTB ; MAX ; CHURC1-FNTB ; MIR4706
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517

2012
dbSNP: rs12435835
rs12435835
FNTB ; MAX ; CHURC1-FNTB
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517

2012
dbSNP: rs12435835
rs12435835
FNTB ; MAX ; CHURC1-FNTB
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASDB Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010

2009
dbSNP: rs2296316
rs2296316
FNTB ; MAX ; CHURC1-FNTB
CUI: C0005890
Disease: Body Height
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs2296322
rs2296322
FNTB ; MAX ; CHURC1-FNTB
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517

2012
dbSNP: rs2412065
rs2412065
GPX2 ; CHURC1 ; CHURC1-FNTB
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 GeneticVariation GWASDB The combination of a genome-wide association study of lymphocyte count and analysis of gene expression data reveals novel asthma candidate genes. 22286170

2012
dbSNP: rs28886684
rs28886684
FNTB ; MAX ; CHURC1-FNTB
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs2898885
rs2898885
RAB15 ; CHURC1-FNTB
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722

2019
dbSNP: rs4466998
rs4466998
FNTB ; MAX ; CHURC1-FNTB
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517

2012
dbSNP: rs4586342
rs4586342
FNTB ; MAX ; CHURC1-FNTB
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517

2012