Source: BEFREE

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: rs744166
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.870 1.000 7 2008 2016
dbSNP: rs744166
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.820 1.000 2 2010 2012
dbSNP: rs9891119
rs9891119
STAT3
0.882 0.120 17 42355962 intron variant A/C snv 0.36
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.810 1.000 1 2013 2013
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: rs744166
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.030 1.000 3 2012 2014
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: rs113994136
rs113994136
STAT3
0.827 0.240 17 42329642 missense variant C/A;T snv
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.020 1.000 2 2011 2011
dbSNP: rs113994136
rs113994136
STAT3
0.827 0.240 17 42329642 missense variant C/A;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.020 1.000 2 2011 2016
dbSNP: rs113994136
rs113994136
STAT3
0.827 0.240 17 42329642 missense variant C/A;T snv
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.020 1.000 2 2011 2013
dbSNP: rs2293152
rs2293152
STAT3
0.763 0.480 17 42329511 intron variant G/A;C;T snv 2.8E-05; 0.59; 1.6E-05
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.020 1.000 2 2014 2016
dbSNP: rs2293152
rs2293152
STAT3
0.763 0.480 17 42329511 intron variant G/A;C;T snv 2.8E-05; 0.59; 1.6E-05
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.020 1.000 2 2012 2014
dbSNP: rs2293152
rs2293152
STAT3
0.763 0.480 17 42329511 intron variant G/A;C;T snv 2.8E-05; 0.59; 1.6E-05
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.020 0.500 2 2013 2015
dbSNP: rs4796793
rs4796793
STAT3
0.716 0.320 17 42390192 upstream gene variant G/C snv 0.67
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.020 1.000 2 2016 2016
dbSNP: rs4796793
rs4796793
STAT3
0.716 0.320 17 42390192 upstream gene variant G/C snv 0.67
CUI: C0278678
Disease: Metastatic Renal Cell Cancer
Metastatic Renal Cell Cancer 		0.020 1.000 2 2016 2016
dbSNP: rs4796793
rs4796793
STAT3
0.716 0.320 17 42390192 upstream gene variant G/C snv 0.67
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.020 1.000 2 2014 2016
dbSNP: rs4796793
rs4796793
STAT3
0.716 0.320 17 42390192 upstream gene variant G/C snv 0.67
CUI: C4721698
Disease: Metastatic Renal Cell Carcinoma
Metastatic Renal Cell Carcinoma 		0.020 1.000 2 2016 2016
dbSNP: rs744166
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.020 1.000 2 2014 2016
dbSNP: rs744166
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease 		0.020 1.000 2 2014 2015
dbSNP: rs744166
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.020 1.000 2 2014 2015
dbSNP: rs744166
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.020 1.000 2 2014 2015
dbSNP: rs747639500
rs747639500
STAT3
1.000 0.120 17 42322402 missense variant C/A snv 7.0E-06
CUI: C1955861
Disease: T-Cell Large Granular Lymphocyte Leukemia
T-Cell Large Granular Lymphocyte Leukemia 		0.020 1.000 2 2014 2016
dbSNP: rs770986654
rs770986654
STAT3
1.000 0.120 17 42322443 missense variant T/A;C snv 4.0E-06
CUI: C1955861
Disease: T-Cell Large Granular Lymphocyte Leukemia
T-Cell Large Granular Lymphocyte Leukemia 		0.020 1.000 2 2014 2018
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