Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs758865880
rs758865880
KYNU
A 0.700 CausalMutation CLINVAR NAD Deficiency, Congenital Malformations, and Niacin Supplementation. 28792876

2017
dbSNP: rs770642379
rs770642379
KYNU
T 0.700 CausalMutation CLINVAR NAD Deficiency, Congenital Malformations, and Niacin Supplementation. 28792876

2017
dbSNP: rs1563322318
rs1563322318
ERI1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs4647924
rs4647924
FGFR3
G 0.700 CausalMutation CLINVAR

dbSNP: rs765379963
rs765379963
TMCO1
A 0.700 CausalMutation CLINVAR

dbSNP: rs767978562
rs767978562
FREM2
T 0.700 CausalMutation CLINVAR

dbSNP: rs121913059
rs121913059
CFH
0.010 GeneticVariation BEFREE We report a case of successful single kidney allograft transplantation in a patient with a CFH gene mutation (R1210C), who had end-stage renal failure after three flares of aHUS treated with plasma exchange. 19633317

2009