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: rs1057521070
rs1057521070
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1970431
Disease:
PITT-HOPKINS SYNDROME
0.700 GeneticVariation UNIPROT
dbSNP: rs1131691735
rs1131691735
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1970431
Disease:
PITT-HOPKINS SYNDROME
A 0.700 CausalMutation CLINVAR
dbSNP: rs1131691735
rs1131691735
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1970431
Disease:
PITT-HOPKINS SYNDROME
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1135401807
rs1135401807
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1970431
Disease:
PITT-HOPKINS SYNDROME
G 0.700 CausalMutation CLINVAR
dbSNP: rs121909122
rs121909122
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1970431
Disease:
PITT-HOPKINS SYNDROME
A 0.700 CausalMutation CLINVAR
dbSNP: rs1555710069
rs1555710069
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1970431
Disease:
PITT-HOPKINS SYNDROME
T 0.700 CausalMutation CLINVAR
dbSNP: rs1555710127
rs1555710127
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1970431
Disease:
PITT-HOPKINS SYNDROME
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555710523
rs1555710523
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1970431
Disease:
PITT-HOPKINS SYNDROME
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555710726
rs1555710726
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1970431
Disease:
PITT-HOPKINS SYNDROME
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555717982
rs1555717982
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1970431
Disease:
PITT-HOPKINS SYNDROME
C 0.700 CausalMutation CLINVAR
dbSNP: rs1555718063
rs1555718063
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1970431
Disease:
PITT-HOPKINS SYNDROME
A 0.700 CausalMutation CLINVAR
dbSNP: rs1555718354
rs1555718354
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1970431
Disease:
PITT-HOPKINS SYNDROME
TCTGGACTA 0.700 GeneticVariation CLINVAR
dbSNP: rs1555718426
rs1555718426
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1970431
Disease:
PITT-HOPKINS SYNDROME
T 0.700 CausalMutation CLINVAR
dbSNP: rs1555721921
rs1555721921
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1970431
Disease:
PITT-HOPKINS SYNDROME
C 0.700 CausalMutation CLINVAR
dbSNP: rs1555722023
rs1555722023
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1970431
Disease:
PITT-HOPKINS SYNDROME
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1555764839
rs1555764839
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1970431
Disease:
PITT-HOPKINS SYNDROME
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1555775233
rs1555775233
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1970431
Disease:
PITT-HOPKINS SYNDROME
TGA 0.700 GeneticVariation CLINVAR
dbSNP: rs1555789019
rs1555789019
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1970431
Disease:
PITT-HOPKINS SYNDROME
GGGAC 0.700 CausalMutation CLINVAR
dbSNP: rs1555796785
rs1555796785
Entrez Id: 6925
Gene Symbol: TCF4
TCF4
CUI: C1970431
Disease:
PITT-HOPKINS SYNDROME
C 0.700 GeneticVariation CLINVAR