Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1135401743
rs1135401743
Entrez Id: 23498;57504
Gene Symbol: HAAO;MTA3
HAAO;MTA3
CUI: C4540004
Disease:
VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 1
T 0.700 CausalMutation CLINVAR NAD Deficiency, Congenital Malformations, and Niacin Supplementation. 28792876 2017