Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7708392
rs7708392
TNIP1
0.010 GeneticVariation BEFREE The C allele of rs7708392 was associated with AIH, especially AIH without DRB1*04:05, an already established risk factor. 29559739

2018