TCF4, transcription factor 4, 6925

N. diseases: 378; N. variants: 111
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909120
rs121909120
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1970431
Disease:
PITT-HOPKINS SYNDROME 		A 0.810 CausalMutation CLINVAR
dbSNP: rs121909121
rs121909121
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1970431
Disease:
PITT-HOPKINS SYNDROME 		T 0.800 GeneticVariation CLINVAR
dbSNP: rs121909121
rs121909121
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1970431
Disease:
PITT-HOPKINS SYNDROME 		T 0.800 CausalMutation CLINVAR
dbSNP: rs121909123
rs121909123
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1970431
Disease:
PITT-HOPKINS SYNDROME 		T 0.800 CausalMutation CLINVAR
dbSNP: rs121909123
rs121909123
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1970431
Disease:
PITT-HOPKINS SYNDROME 		G 0.800 CausalMutation CLINVAR
dbSNP: rs1057518848
rs1057518848
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1970431
Disease:
PITT-HOPKINS SYNDROME 		CATTG 0.700 CausalMutation CLINVAR
dbSNP: rs1057518848
rs1057518848
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1839767
Disease:
Tented upper lip vermilion 		CATTG 0.700 CausalMutation CLINVAR
dbSNP: rs1057518848
rs1057518848
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C0856863
Disease:
Broad-based gait 		CATTG 0.700 CausalMutation CLINVAR
dbSNP: rs1057518848
rs1057518848
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1855330
Disease:
Cerebral hypoplasia 		CATTG 0.700 CausalMutation CLINVAR
dbSNP: rs1057518848
rs1057518848
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1850629
Disease:
Exaggerated cupid's bow 		CATTG 0.700 CausalMutation CLINVAR
dbSNP: rs1057518848
rs1057518848
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1854882
Disease:
Absent speech 		CATTG 0.700 CausalMutation CLINVAR
dbSNP: rs1057518848
rs1057518848
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C0423224
Disease:
Sunken eyes 		CATTG 0.700 CausalMutation CLINVAR
dbSNP: rs1057518848
rs1057518848
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C0557874
Disease:
Global developmental delay 		CATTG 0.700 CausalMutation CLINVAR
dbSNP: rs1057518848
rs1057518848
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C0423109
Disease:
Upward slant of palpebral fissure 		CATTG 0.700 CausalMutation CLINVAR
dbSNP: rs1057518848
rs1057518848
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C0038379
Disease:
Strabismus 		CATTG 0.700 CausalMutation CLINVAR
dbSNP: rs1057518848
rs1057518848
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C0426430
Disease:
Drooping nasal tip 		CATTG 0.700 CausalMutation CLINVAR
dbSNP: rs1057518848
rs1057518848
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1842060
Disease:
Prominent supraorbital ridges 		CATTG 0.700 CausalMutation CLINVAR
dbSNP: rs1057518848
rs1057518848
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C0424731
Disease:
Single transverse palmar crease 		CATTG 0.700 CausalMutation CLINVAR
dbSNP: rs1057518848
rs1057518848
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C0036857
Disease:
Severe intellectual disability 		CATTG 0.700 CausalMutation CLINVAR
dbSNP: rs1057518848
rs1057518848
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C0027092
Disease:
Myopia 		CATTG 0.700 CausalMutation CLINVAR
dbSNP: rs1057518864
rs1057518864
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C0557874
Disease:
Global developmental delay 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1057518864
rs1057518864
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1854114
Disease:
Short nose 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1057518864
rs1057518864
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C0038273
Disease:
Stereotypic Movement Disorder 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1057518864
rs1057518864
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C2674608
Disease:
Feeding difficulties in infancy 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1057518864
rs1057518864
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C0678230
Disease:
Congenital Epicanthus 		T 0.700 CausalMutation CLINVAR