TCF21, transcription factor 21, 6943

N. diseases: 143; N. variants: 6
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12190287
rs12190287 		0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs12190287
rs12190287 		0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs12190287
rs12190287 		0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv
CUI: C0029463
Disease: Osteosarcoma
Osteosarcoma 		Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs12190287
rs12190287 		0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv
CUI: C0585442
Disease: Osteosarcoma of bone
Osteosarcoma of bone 		Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs2327429
rs2327429 		0.882 0.120 6 133888699 non coding transcript exon variant T/C snv 0.24
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs12190287
rs12190287 		0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.010 1.000 1 2017 2017