Variant: rs758865880 

    present in Gene: KYNU
    present in Chromosome: 2
    Position on Chromosome: 142956235
    Alleles of this Variant: T/A

rs758865880 in KYNU gene and Defect of vertebral segmentation PMID 28792876 2017 NAD Deficiency, Congenital Malformations, and Niacin Supplementation.

rs758865880 in KYNU gene and Delayed speech and language development PMID 28792876 2017 NAD Deficiency, Congenital Malformations, and Niacin Supplementation.

rs758865880 in KYNU gene and Frontal bossing PMID 28792876 2017 NAD Deficiency, Congenital Malformations, and Niacin Supplementation.

rs758865880 in KYNU gene and Hypoplastic Left Heart Syndrome PMID 28792876 2017 NAD Deficiency, Congenital Malformations, and Niacin Supplementation.

rs758865880 in KYNU gene and Hypothyroidism PMID 28792876 2017 NAD Deficiency, Congenital Malformations, and Niacin Supplementation.

rs758865880 in KYNU gene and Short long bone PMID 28792876 2017 NAD Deficiency, Congenital Malformations, and Niacin Supplementation.

rs758865880 in KYNU gene and Unilateral agenesis of kidney PMID 28792876 2017 NAD Deficiency, Congenital Malformations, and Niacin Supplementation.