Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs776035233
rs776035233
LCAT
T 0.700 CausalMutation CLINVAR Identification and functional analysis of missense mutations in the lecithin cholesterol acyltransferase gene in a Chilean patient with hypoalphalipoproteinemia. 31164121

2019
dbSNP: rs779114194
rs779114194
LCAT
C 0.700 CausalMutation CLINVAR Identification and functional analysis of missense mutations in the lecithin cholesterol acyltransferase gene in a Chilean patient with hypoalphalipoproteinemia. 31164121

2019
dbSNP: rs1057518781
rs1057518781
MCOLN1
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518782
rs1057518782
MCOLN1 ; LOC105372261
G 0.700 GeneticVariation CLINVAR

dbSNP: rs267607093
rs267607093
SRD5A3
A 0.700 CausalMutation CLINVAR