Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs879255677
rs879255677
MPRIP ; FLCN
TGCGGCTGCGTGGACCTC 0.700 CausalMutation CLINVAR A new locus-specific database (LSDB) for mutations in the folliculin (FLCN) gene. 19802896

2010
dbSNP: rs879255677
rs879255677
MPRIP ; FLCN
TGCGGCTGCGTGGACCTC 0.700 CausalMutation CLINVAR Familial non-VHL clear cell (conventional) renal cell carcinoma: clinical features, segregation analysis, and mutation analysis of FLCN. 18794106

2008