Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10910937
rs10910937
CACNA1E ; LOC107985232
C 0.700 GeneticVariation GWASCAT Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect. 30098192

2018
dbSNP: rs116450688
rs116450688 		G 0.700 GeneticVariation GWASCAT Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect. 30098192

2018
dbSNP: rs13434070
rs13434070
LOC105374016
C 0.700 GeneticVariation GWASCAT Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect. 30098192

2018
dbSNP: rs150579085
rs150579085 		C 0.700 GeneticVariation GWASCAT Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect. 30098192

2018
dbSNP: rs72922085
rs72922085 		G 0.700 GeneticVariation GWASCAT Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect. 30098192

2018
dbSNP: rs201431517
rs201431517
MTFMT
A 0.700 CausalMutation CLINVAR Phenotypic spectrum of eleven patients and five novel MTFMT mutations identified by exome sequencing and candidate gene screening. 24461907

2014
dbSNP: rs201431517
rs201431517
MTFMT
A 0.700 CausalMutation CLINVAR Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translation. 21907147

2011
dbSNP: rs1057518829
rs1057518829
CACNA1F
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518843
rs1057518843
GALC
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1085307139
rs1085307139
PUF60 ; SCRIB
GC 0.700 GeneticVariation CLINVAR

dbSNP: rs1085307993
rs1085307993
GABRB2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs113994152
rs113994152
TSEN54
T 0.700 CausalMutation CLINVAR

dbSNP: rs114925667
rs114925667
UBA5 ; NPHP3-ACAD11
A 0.700 CausalMutation CLINVAR

dbSNP: rs137854539
rs137854539
GNAS
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1554110735
rs1554110735
TFAP2A
C 0.700 CausalMutation CLINVAR

dbSNP: rs1554210073
rs1554210073
PHIP
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555038111
rs1555038111
KMT2A
G 0.700 CausalMutation CLINVAR

dbSNP: rs1555745467
rs1555745467
CACNA1A
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1562114190
rs1562114190
PHIP ; IRAK1BP1
G 0.700 CausalMutation CLINVAR

dbSNP: rs1562127631
rs1562127631
PHIP ; IRAK1BP1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1562134961
rs1562134961
PHIP ; IRAK1BP1
C 0.700 CausalMutation CLINVAR

dbSNP: rs202160208
rs202160208
GMPPB
T 0.700 CausalMutation CLINVAR

dbSNP: rs374052333
rs374052333
UBA5 ; NPHP3-ACAD11
T 0.700 GeneticVariation CLINVAR

dbSNP: rs377274761
rs377274761
GALC
T 0.700 GeneticVariation CLINVAR

dbSNP: rs397507531
rs397507531
PTPN11
C 0.700 CausalMutation CLINVAR