TCF3, transcription factor 3, 6929

N. diseases: 244; N. variants: 8
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: rs1860661
rs1860661 		0.882 0.120 19 1650135 intron variant A/C;G snv 6.7E-06; 0.54
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.810 1.000 1 2014 2014
dbSNP: rs77866734
rs77866734 		1.000 0.040 19 1637053 intron variant C/T snv 1.3E-02
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2016 2016
dbSNP: rs376780559
rs376780559 		1.000 0.080 19 1650226 missense variant G/A snv 8.3E-05 7.7E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.700 0
dbSNP: rs879255271
rs879255271 		1.000 19 1612357 missense variant C/T snv
CUI: C4310786
Disease: AGAMMAGLOBULINEMIA 8, AUTOSOMAL DOMINANT
AGAMMAGLOBULINEMIA 8, AUTOSOMAL DOMINANT 		0.700 0
dbSNP: rs1052918
rs1052918 		1.000 0.080 19 1609670 3 prime UTR variant T/A;C snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs1378286181
rs1378286181 		1.000 0.120 19 1632076 missense variant C/G snv 7.0E-06
CUI: C0595989
Disease: Carcinoma of larynx
Carcinoma of larynx 		Neoplasms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 1994 1994
dbSNP: rs1860661
rs1860661 		0.882 0.120 19 1650135 intron variant A/C;G snv 6.7E-06; 0.54
CUI: C0220597
Disease: Adult Hodgkin Lymphoma
Adult Hodgkin Lymphoma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1860661
rs1860661 		0.882 0.120 19 1650135 intron variant A/C;G snv 6.7E-06; 0.54
CUI: C0220644
Disease: Childhood Hodgkin Lymphoma
Childhood Hodgkin Lymphoma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs368163858
rs368163858 		1.000 0.040 19 1627376 missense variant C/T snv 2.5E-05 2.1E-05
CUI: C0014175
Disease: Endometriosis
Endometriosis 		Female Urogenital Diseases and Pregnancy Complications 0.010 < 0.001 1 2012 2012
dbSNP: rs547275481
rs547275481 		1.000 0.040 19 1621886 missense variant C/T snv 4.2E-05
CUI: C0017638
Disease: Glioma
Glioma 		Neoplasms 0.010 1.000 1 2016 2016