Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7385804
rs7385804
Entrez Id: 7036
Gene Symbol: TFR2
TFR2
CUI: C0014772
Disease:
Red Blood Cell Count measurement
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs62482241
rs62482241
Entrez Id: 7036
Gene Symbol: TFR2
TFR2
CUI: C0014772
Disease:
Red Blood Cell Count measurement
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs2075672
rs2075672
Entrez Id: 7036;51412
Gene Symbol: TFR2;ACTL6B
TFR2;ACTL6B
CUI: C0014772
Disease:
Red Blood Cell Count measurement
A 0.700 GeneticVariation GWASCAT Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos. 28453575 2017
dbSNP: rs2075672
rs2075672
Entrez Id: 7036;51412
Gene Symbol: TFR2;ACTL6B
TFR2;ACTL6B
CUI: C0014772
Disease:
Red Blood Cell Count measurement
0.700 GeneticVariation GWASCAT Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis. 28017375 2017
dbSNP: rs7385804
rs7385804
Entrez Id: 7036
Gene Symbol: TFR2
TFR2
CUI: C0014772
Disease:
Red Blood Cell Count measurement
A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2075672
rs2075672
Entrez Id: 7036;51412
Gene Symbol: TFR2;ACTL6B
TFR2;ACTL6B
CUI: C0014772
Disease:
Red Blood Cell Count measurement
A 0.700 GeneticVariation GWASCAT Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs7385804
rs7385804
Entrez Id: 7036
Gene Symbol: TFR2
TFR2
CUI: C0014772
Disease:
Red Blood Cell Count measurement
C 0.700 GeneticVariation GWASCAT A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. 19820697 2009