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: rs374465594
rs374465594
IL2
4 122451789 missense variant A/G snv 4.1E-06 7.0E-06
CUI: C0010823
Disease: Cytomegalovirus Infections
Cytomegalovirus Infections 		0.010 1.000 1 2012 2012
dbSNP: rs2069778
rs2069778
IL2
1.000 0.080 4 122454980 intron variant G/A snv 0.10
CUI: C0280856
Disease: Squamous cell carcinoma of vulva
Squamous cell carcinoma of vulva 		0.010 1.000 1 2008 2008
dbSNP: rs2069763
rs2069763
IL2
0.807 0.320 4 122456327 synonymous variant C/A snv 0.36 0.29
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.010 1.000 1 2008 2008
dbSNP: rs2069763
rs2069763
IL2
0.807 0.320 4 122456327 synonymous variant C/A snv 0.36 0.29
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.010 1.000 1 2012 2012
dbSNP: rs2069763
rs2069763
IL2
0.807 0.320 4 122456327 synonymous variant C/A snv 0.36 0.29
CUI: C0241910
Disease: Autoimmune Chronic Hepatitis
Autoimmune Chronic Hepatitis 		0.010 1.000 1 2018 2018
dbSNP: rs2069763
rs2069763
IL2
0.807 0.320 4 122456327 synonymous variant C/A snv 0.36 0.29
CUI: C4721555
Disease: Autoimmune hepatitis
Autoimmune hepatitis 		0.010 1.000 1 2018 2018
dbSNP: rs2069763
rs2069763
IL2
0.807 0.320 4 122456327 synonymous variant C/A snv 0.36 0.29
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.010 1.000 1 2008 2008
dbSNP: rs2069762
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary 		0.010 1.000 1 2016 2016
dbSNP: rs2069762
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.010 1.000 1 2009 2009
dbSNP: rs2069762
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia 		0.010 1.000 1 2018 2018
dbSNP: rs2069762
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.010 1.000 1 2010 2010
dbSNP: rs2069762
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0015230
Disease: Exanthema
Exanthema 		0.010 1.000 1 2019 2019
dbSNP: rs2069762
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0271907
Disease: Acquired aplastic anemia
Acquired aplastic anemia 		0.010 < 0.001 1 2017 2017
dbSNP: rs2069762
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.010 1.000 1 2011 2011
dbSNP: rs2069762
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C1302547
Disease: Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma 		0.010 1.000 1 2015 2015
dbSNP: rs2069762
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0241910
Disease: Autoimmune Chronic Hepatitis
Autoimmune Chronic Hepatitis 		0.010 < 0.001 1 2018 2018
dbSNP: rs2069762
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 1.000 1 2010 2010
dbSNP: rs2069762
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0280856
Disease: Squamous cell carcinoma of vulva
Squamous cell carcinoma of vulva 		0.010 1.000 1 2008 2008
dbSNP: rs2069762
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs2069762
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 1.000 1 2017 2017
dbSNP: rs2069762
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 1.000 1 2017 2017
dbSNP: rs2069762
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0019069
Disease: Hemophilia A
Hemophilia A 		0.010 < 0.001 1 2018 2018
dbSNP: rs2069762
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia 		0.010 1.000 1 2018 2018
dbSNP: rs2069762
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		0.010 1.000 1 2020 2020
dbSNP: rs2069762
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.010 1.000 1 2015 2015