TCF21, transcription factor 21, 6943

N. diseases: 143; N. variants: 6
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2327429
rs2327429
Entrez Id: 6943;100507308
Gene Symbol: TCF21;TARID
TCF21;TARID
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE The purpose of this study is to investigate whether TCF21 genetic polymorphisms(rs2327429 T>C, rs2327430 T>C, rs2327433 A>G, rs12190287 C>G, rs7766238 G>A, rs4896011 T>A) are associated with the risk of breast cancer in Chinese women. 27270650 2016
dbSNP: rs2327429
rs2327429
Entrez Id: 6943;100507308
Gene Symbol: TCF21;TARID
TCF21;TARID
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE The purpose of this study is to investigate whether TCF21 genetic polymorphisms(rs2327429 T>C, rs2327430 T>C, rs2327433 A>G, rs12190287 C>G, rs7766238 G>A, rs4896011 T>A) are associated with the risk of breast cancer in Chinese women. 27270650 2016
dbSNP: rs2327430
rs2327430
Entrez Id: 6943;100507308
Gene Symbol: TCF21;TARID
TCF21;TARID
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE The purpose of this study is to investigate whether TCF21 genetic polymorphisms(rs2327429 T>C, rs2327430 T>C, rs2327433 A>G, rs12190287 C>G, rs7766238 G>A, rs4896011 T>A) are associated with the risk of breast cancer in Chinese women. 27270650 2016
dbSNP: rs2327430
rs2327430
Entrez Id: 6943;100507308
Gene Symbol: TCF21;TARID
TCF21;TARID
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE The purpose of this study is to investigate whether TCF21 genetic polymorphisms(rs2327429 T>C, rs2327430 T>C, rs2327433 A>G, rs12190287 C>G, rs7766238 G>A, rs4896011 T>A) are associated with the risk of breast cancer in Chinese women. 27270650 2016
dbSNP: rs2327433
rs2327433
Entrez Id: 6943
Gene Symbol: TCF21
TCF21
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE The purpose of this study is to investigate whether TCF21 genetic polymorphisms(rs2327429 T>C, rs2327430 T>C, rs2327433 A>G, rs12190287 C>G, rs7766238 G>A, rs4896011 T>A) are associated with the risk of breast cancer in Chinese women. 27270650 2016
dbSNP: rs2327433
rs2327433
Entrez Id: 6943
Gene Symbol: TCF21
TCF21
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE The purpose of this study is to investigate whether TCF21 genetic polymorphisms(rs2327429 T>C, rs2327430 T>C, rs2327433 A>G, rs12190287 C>G, rs7766238 G>A, rs4896011 T>A) are associated with the risk of breast cancer in Chinese women. 27270650 2016
dbSNP: rs4896011
rs4896011
Entrez Id: 6943
Gene Symbol: TCF21
TCF21
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE The purpose of this study is to investigate whether TCF21 genetic polymorphisms(rs2327429 T>C, rs2327430 T>C, rs2327433 A>G, rs12190287 C>G, rs7766238 G>A, rs4896011 T>A) are associated with the risk of breast cancer in Chinese women. 27270650 2016
dbSNP: rs4896011
rs4896011
Entrez Id: 6943
Gene Symbol: TCF21
TCF21
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE The purpose of this study is to investigate whether TCF21 genetic polymorphisms(rs2327429 T>C, rs2327430 T>C, rs2327433 A>G, rs12190287 C>G, rs7766238 G>A, rs4896011 T>A) are associated with the risk of breast cancer in Chinese women. 27270650 2016
dbSNP: rs7766238
rs7766238
Entrez Id: 6943
Gene Symbol: TCF21
TCF21
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE The purpose of this study is to investigate whether TCF21 genetic polymorphisms(rs2327429 T>C, rs2327430 T>C, rs2327433 A>G, rs12190287 C>G, rs7766238 G>A, rs4896011 T>A) are associated with the risk of breast cancer in Chinese women. 27270650 2016
dbSNP: rs7766238
rs7766238
Entrez Id: 6943
Gene Symbol: TCF21
TCF21
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE The purpose of this study is to investigate whether TCF21 genetic polymorphisms(rs2327429 T>C, rs2327430 T>C, rs2327433 A>G, rs12190287 C>G, rs7766238 G>A, rs4896011 T>A) are associated with the risk of breast cancer in Chinese women. 27270650 2016
dbSNP: rs12190287
rs12190287
Entrez Id: 6943
Gene Symbol: TCF21
TCF21
CUI: C0027051
Disease:
Myocardial Infarction
0.010 GeneticVariation BEFREE After age, sex, and BMI adjustment, we observed the SNPs rs12190287, rs12413409, rs1412444, rs1746048 and rs4977574, were significantly associated with MI in additive models and rs12190287, rs12413409, rs4977574 were significantly associated with phenotypes of MI at the same time. 24475106 2014
dbSNP: rs12190287
rs12190287
Entrez Id: 6943
Gene Symbol: TCF21
TCF21
CUI: C0003850
Disease:
Arteriosclerosis
0.010 GeneticVariation BEFREE The present study attempted to replicate the results for eight of these loci, CDKN2A/B(rs1333049), ADTRP(rs6903956), PDGFD(rs974819), TCF21(rs12190287), COL4A1-A2(rs4773144), HHIPL1(rs2895811), ADAMTS7(rs4380028) and UBE2Z(rs46522), in patients with pathologically defined atherosclerosis of the coronary arteries. 24573017 2014
dbSNP: rs12190287
rs12190287
Entrez Id: 6943
Gene Symbol: TCF21
TCF21
CUI: C0004153
Disease:
Atherosclerosis
0.010 GeneticVariation BEFREE The present study attempted to replicate the results for eight of these loci, CDKN2A/B(rs1333049), ADTRP(rs6903956), PDGFD(rs974819), TCF21(rs12190287), COL4A1-A2(rs4773144), HHIPL1(rs2895811), ADAMTS7(rs4380028) and UBE2Z(rs46522), in patients with pathologically defined atherosclerosis of the coronary arteries. 24573017 2014