Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1135401744
rs1135401744
T 0.700 CausalMutation CLINVAR NAD Deficiency, Congenital Malformations, and Niacin Supplementation. 28792876

2017

dbSNP: rs527656756
rs527656756
CA 0.700 CausalMutation CLINVAR NAD Deficiency, Congenital Malformations, and Niacin Supplementation. 28792876

2017

dbSNP: rs1014959895
rs1014959895
T 0.700 CausalMutation CLINVAR

dbSNP: rs1251713297
rs1251713297
A 0.700 CausalMutation CLINVAR

dbSNP: rs1554844486
rs1554844486
G 0.700 GeneticVariation CLINVAR

dbSNP: rs368869806
rs368869806
T 0.700 CausalMutation CLINVAR

dbSNP: rs1799945
rs1799945
0.010 GeneticVariation BEFREE Compound heterozygote (C282Y/H63D) of hereditary hemochromatosis in a 16-year-old girl with hypoplastic kidney. 17483072

2007

dbSNP: rs1800562
rs1800562
0.010 GeneticVariation BEFREE Compound heterozygote (C282Y/H63D) of hereditary hemochromatosis in a 16-year-old girl with hypoplastic kidney. 17483072

2007