Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80216136
rs80216136
Entrez Id: 84181
Gene Symbol: CHD6
CHD6
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1010305
rs1010305
Entrez Id: 84181
Gene Symbol: CHD6
CHD6
CUI: C1445957
Disease:
Serum total cholesterol measurement 		A 0.700 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531 2018
dbSNP: rs4142393
rs4142393
Entrez Id: 84181
Gene Symbol: CHD6
CHD6
CUI: C1445957
Disease:
Serum total cholesterol measurement 		T 0.700 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531 2018
dbSNP: rs6029691
rs6029691
Entrez Id: 84181
Gene Symbol: CHD6
CHD6
CUI: C0004106
Disease:
Astigmatism 		C 0.700 GeneticVariation GWASCAT Genome-wide association studies for corneal and refractive astigmatism in UK Biobank demonstrate a shared role for myopia susceptibility loci. 30306274 2018
dbSNP: rs73611298
rs73611298
Entrez Id: 84181
Gene Symbol: CHD6
CHD6
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219 2012