Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893805
rs104893805
0.800 GeneticVariation UNIPROT Molecular findings and clinical data in a cohort of 150 patients with anophthalmia/microphthalmia. 24033328

2014

dbSNP: rs104893805
rs104893805
0.800 GeneticVariation UNIPROT Mutations in SOX2 cause anophthalmia. 12612584

2003

dbSNP: rs104893805
rs104893805
C 0.800 CausalMutation CLINVAR

dbSNP: rs1560264973
rs1560264973
ACCTCGG 0.700 CausalMutation CLINVAR A novel heterozygous SOX2 mutation causing congenital bilateral anophthalmia, hypogonadotropic hypogonadism and growth hormone deficiency. 24211324

2014

dbSNP: rs1560264973
rs1560264973
ACCTCGG 0.700 CausalMutation CLINVAR Clinical and mutation analysis of 51 probands with anophthalmia and/or severe microphthalmia from a single center. 24498598

2013

dbSNP: rs771521201
rs771521201
G 0.700 CausalMutation CLINVAR Parent-of-origin effects in SOX2 anophthalmia syndrome. 22171155

2011

dbSNP: rs1560264973
rs1560264973
ACCTCGG 0.700 CausalMutation CLINVAR Novel SOX2 mutations and genotype-phenotype correlation in anophthalmia and microphthalmia. 19921648

2009

dbSNP: rs771521201
rs771521201
G 0.700 CausalMutation CLINVAR Novel SOX2 mutations and genotype-phenotype correlation in anophthalmia and microphthalmia. 19921648

2009

dbSNP: rs104893799
rs104893799
T 0.700 CausalMutation CLINVAR

dbSNP: rs104893800
rs104893800
T 0.700 CausalMutation CLINVAR

dbSNP: rs104893801
rs104893801
A 0.700 CausalMutation CLINVAR

dbSNP: rs104893802
rs104893802
C 0.700 CausalMutation CLINVAR

dbSNP: rs104893803
rs104893803
T 0.700 CausalMutation CLINVAR

dbSNP: rs104893804
rs104893804
T 0.700 CausalMutation CLINVAR

dbSNP: rs104893806
rs104893806
G 0.700 CausalMutation CLINVAR

dbSNP: rs1553862958
rs1553862958
TC 0.700 CausalMutation CLINVAR

dbSNP: rs1553862971
rs1553862971
C 0.700 CausalMutation CLINVAR

dbSNP: rs1560264167
rs1560264167
GGGCGGCGGCGGCAACTCCACCGC 0.700 CausalMutation CLINVAR

dbSNP: rs1560264452
rs1560264452
C 0.700 CausalMutation CLINVAR

dbSNP: rs387906688
rs387906688
A 0.700 CausalMutation CLINVAR

dbSNP: rs398122803
rs398122803
CGG 0.700 CausalMutation CLINVAR

dbSNP: rs398122915
rs398122915
AA 0.700 CausalMutation CLINVAR

dbSNP: rs398122916
rs398122916
T 0.700 CausalMutation CLINVAR

dbSNP: rs587776776
rs587776776
A 0.700 CausalMutation CLINVAR