Gene: INF2 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs530391015
rs530391015
INF2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1186292917
rs1186292917
INF2
0.010 GeneticVariation BEFREE The first (p.Arg214His) was identified in the FSGS patient with a positive family history. 30126379

2018
dbSNP: rs267606879
rs267606879
INF2
0.010 GeneticVariation BEFREE The first (p.Arg214His) was identified in the FSGS patient with a positive family history. 30126379

2018
dbSNP: rs754313620
rs754313620
INF2
0.010 GeneticVariation BEFREE In the present study, a mutation in TRNL1 (m. 3290T>C) was identified, which was the first reported variant associated with FSGS. 29138824

2018