Condition: Vitamin D Deficiency


rs1428826948 in APOL1 gene and Vitamin D Deficiency PMID 20647424 2010 Association of trypanolytic ApoL1 variants with kidney disease in African Americans.

rs10741657 in CYP2R1 gene and Vitamin D Deficiency PMID 20541252 2010 Common genetic determinants of vitamin D insufficiency: a genome-wide association study.

rs2282679 in GC gene and Vitamin D Deficiency PMID 20541252 2010 Common genetic determinants of vitamin D insufficiency: a genome-wide association study.

rs151344517 in LOC107985154;AFG3L2;TUBB6 gene and Vitamin D Deficiency PMID 20725928 2010 Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias.

rs12785878 in NADSYN1 gene and Vitamin D Deficiency PMID 20541252 2010 Common genetic determinants of vitamin D insufficiency: a genome-wide association study.