Variant: rs1135401743 

    present in Gene: HAAO;MTA3
    present in Chromosome: 2
    Position on Chromosome: 42769785
    Alleles of this Variant: C/A;T

rs1135401743 in HAAO;MTA3 gene and Abnormality of the ribs PMID 28792876 2017 NAD Deficiency, Congenital Malformations, and Niacin Supplementation.

rs1135401743 in HAAO;MTA3 gene and Allanson Pantzar McLeod syndrome PMID 28792876 2017 NAD Deficiency, Congenital Malformations, and Niacin Supplementation.

rs1135401743 in HAAO;MTA3 gene and Butterfly vertebrae PMID 28792876 2017 NAD Deficiency, Congenital Malformations, and Niacin Supplementation.

rs1135401743 in HAAO;MTA3 gene and Defect of vertebral segmentation PMID 28792876 2017 NAD Deficiency, Congenital Malformations, and Niacin Supplementation.

rs1135401743 in HAAO;MTA3 gene and Hypoplastic Left Heart Syndrome PMID 28792876 2017 NAD Deficiency, Congenital Malformations, and Niacin Supplementation.

rs1135401743 in HAAO;MTA3 gene and Hypoplastic sacrum PMID 28792876 2017 NAD Deficiency, Congenital Malformations, and Niacin Supplementation.

rs1135401743 in HAAO;MTA3 gene and Sensorineural Hearing Loss (disorder) PMID 28792876 2017 NAD Deficiency, Congenital Malformations, and Niacin Supplementation.

rs1135401743 in HAAO;MTA3 gene and Short 1st metacarpal PMID 28792876 2017 NAD Deficiency, Congenital Malformations, and Niacin Supplementation.

rs1135401743 in HAAO;MTA3 gene and Spina Bifida PMID 28792876 2017 NAD Deficiency, Congenital Malformations, and Niacin Supplementation.

rs1135401743 in HAAO;MTA3 gene and Tethered Cord Syndrome PMID 28792876 2017 NAD Deficiency, Congenital Malformations, and Niacin Supplementation.

rs1135401743 in HAAO;MTA3 gene and VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 1 PMID 28792876 2017 NAD Deficiency, Congenital Malformations, and Niacin Supplementation.