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.