Disease: Familial (FPAH) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs55916807
rs55916807
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C1611743
Disease:
Familial (FPAH) 		0.010 GeneticVariation BEFREE Furthermore, the mutated alleles R20C and R72H did not segregate with the SLE phenotype in familial cases of SLE. 17464555 2007