Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10194817
rs10194817
Entrez Id: 2281;80304;388931
Gene Symbol: FKBP1B;WDCP;MFSD2B
FKBP1B;WDCP;MFSD2B
CUI: C0427460
Disease:
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs10194817
rs10194817
Entrez Id: 2281;80304;388931
Gene Symbol: FKBP1B;WDCP;MFSD2B
FKBP1B;WDCP;MFSD2B
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: rs75745192
rs75745192
Entrez Id: 2281;80304;388931
Gene Symbol: FKBP1B;WDCP;MFSD2B
FKBP1B;WDCP;MFSD2B
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs4665652
rs4665652
Entrez Id: 388931
Gene Symbol: MFSD2B
MFSD2B
CUI: C0005890
Disease:
Body Height 		A 0.700 GeneticVariation GWASCAT Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. 28552196 2017
dbSNP: rs70944707
rs70944707
Entrez Id: 2281;80304;388931
Gene Symbol: FKBP1B;WDCP;MFSD2B
FKBP1B;WDCP;MFSD2B
CUI: C0008810
Disease:
Circadian Rhythms 		C 0.700 GeneticVariation GWASCAT Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci. 27494321 2016
dbSNP: rs72781680
rs72781680
Entrez Id: 388931
Gene Symbol: MFSD2B
MFSD2B
CUI: C0200635
Disease:
Lymphocyte Count measurement 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs7561675
rs7561675
Entrez Id: 388931
Gene Symbol: MFSD2B
MFSD2B
CUI: C0206161
Disease:
Reticulocyte count (procedure) 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs925228
rs925228
Entrez Id: 388931
Gene Symbol: MFSD2B
MFSD2B
CUI: C0206161
Disease:
Reticulocyte count (procedure) 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016