FOXL2, forkhead box L2, 668

N. diseases: 137; N. variants: 102
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893738
rs104893738
Entrez Id: 668;401089;103344930
Gene Symbol: FOXL2;FOXL2NB;LINC01391
FOXL2;FOXL2NB;LINC01391
CUI: C2931136
Disease:
Blepharophimosis syndrome type 2 		C 0.700 CausalMutation CLINVAR
dbSNP: rs104893739
rs104893739
Entrez Id: 668;401089
Gene Symbol: FOXL2;FOXL2NB
FOXL2;FOXL2NB
CUI: C0220663
Disease:
BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS (disorder) 		A 0.700 CausalMutation CLINVAR
dbSNP: rs104893741
rs104893741
Entrez Id: 668;401089
Gene Symbol: FOXL2;FOXL2NB
FOXL2;FOXL2NB
CUI: C0220663
Disease:
BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS (disorder) 		A 0.700 CausalMutation CLINVAR
dbSNP: rs104893741
rs104893741
Entrez Id: 668;401089
Gene Symbol: FOXL2;FOXL2NB
FOXL2;FOXL2NB
CUI: C2931135
Disease:
Blepharophimosis syndrome type 1 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1057516139
rs1057516139
Entrez Id: 668;401089
Gene Symbol: FOXL2;FOXL2NB
FOXL2;FOXL2NB
CUI: C0220663
Disease:
BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS (disorder) 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1057516140
rs1057516140
Entrez Id: 668;401089
Gene Symbol: FOXL2;FOXL2NB
FOXL2;FOXL2NB
CUI: C0220663
Disease:
BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS (disorder) 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1057516141
rs1057516141
Entrez Id: 668;401089
Gene Symbol: FOXL2;FOXL2NB
FOXL2;FOXL2NB
CUI: C0220663
Disease:
BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS (disorder) 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1057516142
rs1057516142
Entrez Id: 668;401089
Gene Symbol: FOXL2;FOXL2NB
FOXL2;FOXL2NB
CUI: C0220663
Disease:
BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS (disorder) 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1057516142
rs1057516142
Entrez Id: 668;401089
Gene Symbol: FOXL2;FOXL2NB
FOXL2;FOXL2NB
CUI: C0220663
Disease:
BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS (disorder) 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1057516144
rs1057516144
Entrez Id: 668;401089
Gene Symbol: FOXL2;FOXL2NB
FOXL2;FOXL2NB
CUI: C0220663
Disease:
BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS (disorder) 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1057516145
rs1057516145
Entrez Id: 668;401089
Gene Symbol: FOXL2;FOXL2NB
FOXL2;FOXL2NB
CUI: C0220663
Disease:
BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS (disorder) 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1057516149
rs1057516149
Entrez Id: 668;401089
Gene Symbol: FOXL2;FOXL2NB
FOXL2;FOXL2NB
CUI: C0220663
Disease:
BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS (disorder) 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1057516150
rs1057516150
Entrez Id: 668;401089
Gene Symbol: FOXL2;FOXL2NB
FOXL2;FOXL2NB
CUI: C0220663
Disease:
BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS (disorder) 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1057516151
rs1057516151
Entrez Id: 668;401089
Gene Symbol: FOXL2;FOXL2NB
FOXL2;FOXL2NB
CUI: C0220663
Disease:
BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS (disorder) 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1057516153
rs1057516153
Entrez Id: 668;401089
Gene Symbol: FOXL2;FOXL2NB
FOXL2;FOXL2NB
CUI: C0220663
Disease:
BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS (disorder) 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1057516156
rs1057516156
Entrez Id: 668;401089
Gene Symbol: FOXL2;FOXL2NB
FOXL2;FOXL2NB
CUI: C0220663
Disease:
BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS (disorder) 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs1057516157
rs1057516157
Entrez Id: 668;401089
Gene Symbol: FOXL2;FOXL2NB
FOXL2;FOXL2NB
CUI: C0220663
Disease:
BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS (disorder) 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1057516158
rs1057516158
Entrez Id: 668;401089
Gene Symbol: FOXL2;FOXL2NB
FOXL2;FOXL2NB
CUI: C0220663
Disease:
BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS (disorder) 		G 0.700 CausalMutation CLINVAR
dbSNP: rs1057516159
rs1057516159
Entrez Id: 668;401089
Gene Symbol: FOXL2;FOXL2NB
FOXL2;FOXL2NB
CUI: C0220663
Disease:
BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS (disorder) 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1057516161
rs1057516161
Entrez Id: 668;401089
Gene Symbol: FOXL2;FOXL2NB
FOXL2;FOXL2NB
CUI: C0220663
Disease:
BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS (disorder) 		TG 0.700 CausalMutation CLINVAR
dbSNP: rs1057516163
rs1057516163
Entrez Id: 668;401089
Gene Symbol: FOXL2;FOXL2NB
FOXL2;FOXL2NB
CUI: C0220663
Disease:
BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS (disorder) 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1057516164
rs1057516164
Entrez Id: 668;401089
Gene Symbol: FOXL2;FOXL2NB
FOXL2;FOXL2NB
CUI: C0220663
Disease:
BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS (disorder) 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1057516165
rs1057516165
Entrez Id: 668;401089
Gene Symbol: FOXL2;FOXL2NB
FOXL2;FOXL2NB
CUI: C0220663
Disease:
BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS (disorder) 		G 0.700 CausalMutation CLINVAR
dbSNP: rs1057516166
rs1057516166
Entrez Id: 668;401089
Gene Symbol: FOXL2;FOXL2NB
FOXL2;FOXL2NB
CUI: C0220663
Disease:
BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS (disorder) 		AGGAGGCATAGGGCATGGGTGAG 0.700 CausalMutation CLINVAR
dbSNP: rs1057516167
rs1057516167
Entrez Id: 668;401089
Gene Symbol: FOXL2;FOXL2NB
FOXL2;FOXL2NB
CUI: C0220663
Disease:
BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS (disorder) 		T 0.700 CausalMutation CLINVAR