Gene: TCF4 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057521070
rs1057521070
TCF4
T 0.700 CausalMutation CLINVAR A common trinucleotide repeat expansion within the transcription factor 4 (TCF4, E2-2) gene predicts Fuchs corneal dystrophy. 23185296

2012
dbSNP: rs1555710171
rs1555710171
TCF4
A 0.700 GeneticVariation CLINVAR A common trinucleotide repeat expansion within the transcription factor 4 (TCF4, E2-2) gene predicts Fuchs corneal dystrophy. 23185296

2012
dbSNP: rs1555721921
rs1555721921
TCF4
G 0.700 GeneticVariation CLINVAR A common trinucleotide repeat expansion within the transcription factor 4 (TCF4, E2-2) gene predicts Fuchs corneal dystrophy. 23185296

2012
dbSNP: rs1555778204
rs1555778204
TCF4
A 0.700 CausalMutation CLINVAR A common trinucleotide repeat expansion within the transcription factor 4 (TCF4, E2-2) gene predicts Fuchs corneal dystrophy. 23185296

2012
dbSNP: rs1555797248
rs1555797248
TCF4
T 0.700 CausalMutation CLINVAR A common trinucleotide repeat expansion within the transcription factor 4 (TCF4, E2-2) gene predicts Fuchs corneal dystrophy. 23185296

2012
dbSNP: rs1057521070
rs1057521070
TCF4
T 0.700 CausalMutation CLINVAR A loss-of-function mutation in the FTSJ1 gene causes nonsyndromic X-linked mental retardation in a Japanese family. 18081026

2008
dbSNP: rs1555710171
rs1555710171
TCF4
A 0.700 GeneticVariation CLINVAR A loss-of-function mutation in the FTSJ1 gene causes nonsyndromic X-linked mental retardation in a Japanese family. 18081026

2008
dbSNP: rs1555721921
rs1555721921
TCF4
G 0.700 GeneticVariation CLINVAR A loss-of-function mutation in the FTSJ1 gene causes nonsyndromic X-linked mental retardation in a Japanese family. 18081026

2008
dbSNP: rs1555778204
rs1555778204
TCF4
A 0.700 CausalMutation CLINVAR A loss-of-function mutation in the FTSJ1 gene causes nonsyndromic X-linked mental retardation in a Japanese family. 18081026

2008
dbSNP: rs1555797248
rs1555797248
TCF4
T 0.700 CausalMutation CLINVAR A loss-of-function mutation in the FTSJ1 gene causes nonsyndromic X-linked mental retardation in a Japanese family. 18081026

2008
dbSNP: rs1057521070
rs1057521070
TCF4
T 0.700 CausalMutation CLINVAR Association of TCF4 polymorphisms and Fuchs' endothelial dystrophy: a meta-analysis. 26087656

2015
dbSNP: rs1555710171
rs1555710171
TCF4
A 0.700 GeneticVariation CLINVAR Association of TCF4 polymorphisms and Fuchs' endothelial dystrophy: a meta-analysis. 26087656

2015
dbSNP: rs1555721921
rs1555721921
TCF4
G 0.700 GeneticVariation CLINVAR Association of TCF4 polymorphisms and Fuchs' endothelial dystrophy: a meta-analysis. 26087656

2015
dbSNP: rs1555778204
rs1555778204
TCF4
A 0.700 CausalMutation CLINVAR Association of TCF4 polymorphisms and Fuchs' endothelial dystrophy: a meta-analysis. 26087656

2015
dbSNP: rs1555797248
rs1555797248
TCF4
T 0.700 CausalMutation CLINVAR Association of TCF4 polymorphisms and Fuchs' endothelial dystrophy: a meta-analysis. 26087656

2015
dbSNP: rs1057521070
rs1057521070
TCF4
T 0.700 CausalMutation CLINVAR Clinical application of exome sequencing in undiagnosed genetic conditions. 22581936

2012
dbSNP: rs1555710171
rs1555710171
TCF4
A 0.700 GeneticVariation CLINVAR Clinical application of exome sequencing in undiagnosed genetic conditions. 22581936

2012
dbSNP: rs1555721921
rs1555721921
TCF4
G 0.700 GeneticVariation CLINVAR Clinical application of exome sequencing in undiagnosed genetic conditions. 22581936

2012
dbSNP: rs1555778204
rs1555778204
TCF4
A 0.700 CausalMutation CLINVAR Clinical application of exome sequencing in undiagnosed genetic conditions. 22581936

2012
dbSNP: rs1555797248
rs1555797248
TCF4
T 0.700 CausalMutation CLINVAR Clinical application of exome sequencing in undiagnosed genetic conditions. 22581936

2012
dbSNP: rs1057521070
rs1057521070
TCF4
T 0.700 CausalMutation CLINVAR Development, cognition, and behaviour in Pitt-Hopkins syndrome. 22712893

2012
dbSNP: rs1555710171
rs1555710171
TCF4
A 0.700 GeneticVariation CLINVAR Development, cognition, and behaviour in Pitt-Hopkins syndrome. 22712893

2012
dbSNP: rs1555721921
rs1555721921
TCF4
G 0.700 GeneticVariation CLINVAR Development, cognition, and behaviour in Pitt-Hopkins syndrome. 22712893

2012
dbSNP: rs1555778204
rs1555778204
TCF4
A 0.700 CausalMutation CLINVAR Development, cognition, and behaviour in Pitt-Hopkins syndrome. 22712893

2012
dbSNP: rs1555797248
rs1555797248
TCF4
T 0.700 CausalMutation CLINVAR Development, cognition, and behaviour in Pitt-Hopkins syndrome. 22712893

2012