Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121912745
rs121912745
SLC4A1
0.710 GeneticVariation BEFREE Three different mutations at this position (R589C, R589H, and R589S) were all found in AD dRTA and a de novo R589H mutation has previously been recorded. 12750988

2003
dbSNP: rs121912745
rs121912745
SLC4A1
T 0.710 CausalMutation CLINVAR

dbSNP: rs121912745
rs121912745
SLC4A1
A 0.710 CausalMutation CLINVAR