Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104886186
rs104886186
COL4A5
0.710 GeneticVariation BEFREE A single-base mutation in exon 31 converting glycine 852 to arginine in the collagenous domain in an Alport syndrome patient. 8893151

1996
dbSNP: rs104886186
rs104886186
COL4A5
A 0.710 CausalMutation CLINVAR