Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1053004
rs1053004
STAT3
0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.040 0.750 4 2013 2019
dbSNP: rs1053004
rs1053004
STAT3
0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.030 0.667 3 2017 2019
dbSNP: rs1053004
rs1053004
STAT3
0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48
CUI: C0524909
Disease: Hepatitis B, Chronic
Hepatitis B, Chronic 		0.020 1.000 2 2015 2017
dbSNP: rs1053004
rs1053004
STAT3
0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48
CUI: C0151517
Disease: Complete atrioventricular block
Complete atrioventricular block 		0.020 1.000 2 2015 2017
dbSNP: rs1053004
rs1053004
STAT3
0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48
CUI: C0023895
Disease: Liver diseases
Liver diseases 		0.010 1.000 1 2018 2018
dbSNP: rs1053004
rs1053004
STAT3
0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48
CUI: C0349566
Disease: Squamous cell carcinoma of tongue
Squamous cell carcinoma of tongue 		0.010 1.000 1 2019 2019
dbSNP: rs1053004
rs1053004
STAT3
0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2019 2019
dbSNP: rs1053004
rs1053004
STAT3
0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		0.010 1.000 1 2016 2016
dbSNP: rs1053004
rs1053004
STAT3
0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas 		0.010 1.000 1 2016 2016
dbSNP: rs1053004
rs1053004
STAT3
0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs1053004
rs1053004
STAT3
0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48
CUI: C4721579
Disease: Secondary malignant neoplasm of colon and/or rectum
Secondary malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2018 2018
dbSNP: rs1053005
rs1053005
STAT3
0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25
CUI: C0524909
Disease: Hepatitis B, Chronic
Hepatitis B, Chronic 		0.010 1.000 1 2018 2018
dbSNP: rs1053005
rs1053005
STAT3
0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		0.010 1.000 1 2016 2016
dbSNP: rs1053005
rs1053005
STAT3
0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.010 1.000 1 2013 2013
dbSNP: rs1053005
rs1053005
STAT3
0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25
CUI: C0023895
Disease: Liver diseases
Liver diseases 		0.010 1.000 1 2018 2018
dbSNP: rs1053005
rs1053005
STAT3
0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.010 1.000 1 2011 2011
dbSNP: rs1053005
rs1053005
STAT3
0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas 		0.010 1.000 1 2016 2016
dbSNP: rs1053005
rs1053005
STAT3
0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease 		0.010 1.000 1 2013 2013
dbSNP: rs1053005
rs1053005
STAT3
0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.010 1.000 1 2018 2018
dbSNP: rs1053005
rs1053005
STAT3
0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25
CUI: C3840565
Disease: Autoimmune thyroid disease (AITD)
Autoimmune thyroid disease (AITD) 		0.010 1.000 1 2013 2013
dbSNP: rs1053005
rs1053005
STAT3
0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25
CUI: C0028754
Disease: Obesity
Obesity 		0.010 1.000 1 2014 2014
dbSNP: rs1053023
rs1053023
STAT3
0.882 0.120 17 42313598 3 prime UTR variant T/A;C snv
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 1.000 1 2018 2018
dbSNP: rs1053023
rs1053023
STAT3
0.882 0.120 17 42313598 3 prime UTR variant T/A;C snv
CUI: C0079731
Disease: B-Cell Lymphomas
B-Cell Lymphomas 		0.010 1.000 1 2011 2011
dbSNP: rs1053023
rs1053023
STAT3
0.882 0.120 17 42313598 3 prime UTR variant T/A;C snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 1.000 1 2018 2018
dbSNP: rs1053023
rs1053023
STAT3
0.882 0.120 17 42313598 3 prime UTR variant T/A;C snv
CUI: C4552766
Disease: Miscarriage
Miscarriage 		0.010 1.000 1 2010 2010