Gene: FLCN ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs755959303
rs755959303
MPRIP ; FLCN
T 0.700 CausalMutation CLINVAR

dbSNP: rs757197845
rs757197845
MPRIP ; FLCN
CAATCTTAT 0.700 CausalMutation CLINVAR

dbSNP: rs758175953
rs758175953
FLCN
A 0.700 GeneticVariation CLINVAR

dbSNP: rs758385503
rs758385503
FLCN
CG 0.700 CausalMutation CLINVAR

dbSNP: rs786202081
rs786202081
FLCN
T 0.700 CausalMutation CLINVAR

dbSNP: rs786203218
rs786203218
FLCN
T 0.700 GeneticVariation CLINVAR

dbSNP: rs876658390
rs876658390
FLCN
G 0.700 CausalMutation CLINVAR

dbSNP: rs876658409
rs876658409
FLCN
T 0.700 CausalMutation CLINVAR

dbSNP: rs876660611
rs876660611
FLCN
C 0.700 CausalMutation CLINVAR

dbSNP: rs878855214
rs878855214
MPRIP ; FLCN
C 0.700 GeneticVariation CLINVAR

dbSNP: rs878855218
rs878855218
FLCN
G 0.700 GeneticVariation CLINVAR

dbSNP: rs878855218
rs878855218
FLCN
A 0.700 GeneticVariation CLINVAR

dbSNP: rs878855220
rs878855220
FLCN
TCT 0.700 CausalMutation CLINVAR

dbSNP: rs878855221
rs878855221
FLCN
A 0.700 CausalMutation CLINVAR

dbSNP: rs879255658
rs879255658
FLCN
G 0.700 CausalMutation CLINVAR

dbSNP: rs879255660
rs879255660
FLCN
A 0.700 CausalMutation CLINVAR

dbSNP: rs879255661
rs879255661
FLCN
G 0.700 CausalMutation CLINVAR

dbSNP: rs879255662
rs879255662
FLCN
C 0.700 CausalMutation CLINVAR

dbSNP: rs879255663
rs879255663
FLCN
T 0.700 CausalMutation CLINVAR

dbSNP: rs879255666
rs879255666
FLCN
G 0.700 CausalMutation CLINVAR

dbSNP: rs879255667
rs879255667
FLCN
A 0.700 CausalMutation CLINVAR

dbSNP: rs879255668
rs879255668
FLCN
C 0.700 CausalMutation CLINVAR

dbSNP: rs879255669
rs879255669
FLCN
CT 0.700 CausalMutation CLINVAR

dbSNP: rs879255670
rs879255670
FLCN
G 0.700 CausalMutation CLINVAR

dbSNP: rs879255672
rs879255672
MPRIP ; FLCN
T 0.700 CausalMutation CLINVAR