Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs143326447
rs143326447
Entrez Id: 541471;105373557
Gene Symbol: MIR4435-2HG;SOCAR
MIR4435-2HG;SOCAR
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2009581
rs2009581
Entrez Id: 55289;541471
Gene Symbol: ACOXL;MIR4435-2HG
ACOXL;MIR4435-2HG
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2139376
rs2139376
Entrez Id: 541471
Gene Symbol: MIR4435-2HG
MIR4435-2HG
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs604126
rs604126
Entrez Id: 541471
Gene Symbol: MIR4435-2HG
MIR4435-2HG
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs62160676
rs62160676
Entrez Id: 541471
Gene Symbol: MIR4435-2HG
MIR4435-2HG
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs112744032
rs112744032
Entrez Id: 541471;105373557
Gene Symbol: MIR4435-2HG;SOCAR
MIR4435-2HG;SOCAR
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin
A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2334232
rs2334232
Entrez Id: 541471
Gene Symbol: MIR4435-2HG
MIR4435-2HG
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin
A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs4848370
rs4848370
Entrez Id: 55289;541471
Gene Symbol: ACOXL;MIR4435-2HG
ACOXL;MIR4435-2HG
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs616582
rs616582
Entrez Id: 541471
Gene Symbol: MIR4435-2HG
MIR4435-2HG
CUI: C1261502
Disease:
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: rs62160676
rs62160676
Entrez Id: 541471
Gene Symbol: MIR4435-2HG
MIR4435-2HG
CUI: C1261502
Disease:
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