Gene: FOXL2 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057516144
rs1057516144
FOXL2 ; FOXL2NB
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057516145
rs1057516145
FOXL2 ; FOXL2NB
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057516149
rs1057516149
FOXL2 ; FOXL2NB
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057516150
rs1057516150
FOXL2 ; FOXL2NB
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057516151
rs1057516151
FOXL2 ; FOXL2NB
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1057516153
rs1057516153
FOXL2 ; FOXL2NB
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1057516156
rs1057516156
FOXL2 ; FOXL2NB
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057516157
rs1057516157
FOXL2 ; FOXL2NB
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1057516158
rs1057516158
FOXL2 ; FOXL2NB
G 0.700 CausalMutation CLINVAR

dbSNP: rs1057516159
rs1057516159
FOXL2 ; FOXL2NB
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1057516161
rs1057516161
FOXL2 ; FOXL2NB
TG 0.700 CausalMutation CLINVAR

dbSNP: rs1057516163
rs1057516163
FOXL2 ; FOXL2NB
C 0.700 CausalMutation CLINVAR

dbSNP: rs1057516164
rs1057516164
FOXL2 ; FOXL2NB
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057516165
rs1057516165
FOXL2 ; FOXL2NB
G 0.700 CausalMutation CLINVAR

dbSNP: rs1057516166
rs1057516166
FOXL2 ; FOXL2NB
AGGAGGCATAGGGCATGGGTGAG 0.700 CausalMutation CLINVAR

dbSNP: rs1057516167
rs1057516167
FOXL2 ; FOXL2NB
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057516170
rs1057516170
FOXL2 ; FOXL2NB
C 0.700 CausalMutation CLINVAR

dbSNP: rs1057516172
rs1057516172
FOXL2 ; FOXL2NB
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060499717
rs1060499717
FOXL2 ; FOXL2NB
A 0.700 CausalMutation CLINVAR

dbSNP: rs121908359
rs121908359
FOXL2 ; FOXL2NB
T 0.700 CausalMutation CLINVAR

dbSNP: rs1226344391
rs1226344391
FOXL2 ; FOXL2NB
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1315073489
rs1315073489
FOXL2 ; FOXL2NB
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1553752849
rs1553752849
FOXL2 ; FOXL2NB
GGCGGCTGCAGCCGCAGCTGCTGCAGCCGCT 0.700 CausalMutation CLINVAR

dbSNP: rs1553752890
rs1553752890
FOXL2 ; FOXL2NB
GTGCGCGGGCGGCGGCCGGAAGGGCCTCTTCATGCGGCGGCGGCGCCGGTAGTTGCCCTTCTCGAACATGTCTTCGCAGGCCGGGTCCAGCGTCCAGTAGTTGCCCTTGCGCTCGCCGCCGCCCT 0.700 CausalMutation CLINVAR

dbSNP: rs1553752945
rs1553752945
FOXL2 ; FOXL2NB
CT 0.700 CausalMutation CLINVAR