Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121912751
rs121912751
SLC4A1
0.740 GeneticVariation BEFREE Thus impaired trafficking of the kAE1 G701D and A858D mutants would lead to a profound decrease in functional kAE1 at the basolateral membrane of alpha-intercalated cells in the distal nephron of the patients with dRTA. 20151848

2010
dbSNP: rs121912751
rs121912751
SLC4A1
0.740 GeneticVariation BEFREE We report here two unrelated Indian patients with combined hemolytic anemia and dRTA who share homozygous A858D mutations of the AE1/SLC4A1 gene. 20799361

2010
dbSNP: rs121912751
rs121912751
SLC4A1
0.740 GeneticVariation BEFREE Genetic and hematological studies in 18 Thai patients with dRTA have shown that 12 of them (67%) carried SLC4A1 mutations (7 G701D/G701D, 3 SAO/G701D, and 2 G701D/A858D). 18266205

2008
dbSNP: rs121912751
rs121912751
SLC4A1
0.740 GeneticVariation BEFREE Individuals heterozygous with wild-type (WT) kAE1 either did not display any symptoms of dRTA (DeltaV850/WT) or displayed a mild incomplete form of dRTA (A858D/WT), while compound heterozygotes (DeltaV850/A858D) had dRTA. 16849697

2006
dbSNP: rs121912751
rs121912751
SLC4A1
0.740 GeneticVariation UNIPROT