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: rs2221903
rs2221903
0.752 0.360 4 122617757 intron variant C/T snv 0.77
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.030 1.000 3 2008 2015
dbSNP: rs2221903
rs2221903
0.752 0.360 4 122617757 intron variant C/T snv 0.77
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.020 1.000 2 2013 2016
dbSNP: rs2221903
rs2221903
0.752 0.360 4 122617757 intron variant C/T snv 0.77
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.020 1.000 2 2016 2019
dbSNP: rs2221903
rs2221903
0.752 0.360 4 122617757 intron variant C/T snv 0.77
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.010 1.000 1 2017 2017
dbSNP: rs2221903
rs2221903
0.752 0.360 4 122617757 intron variant C/T snv 0.77
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2013 2013
dbSNP: rs2221903
rs2221903
0.752 0.360 4 122617757 intron variant C/T snv 0.77
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.010 1.000 1 2019 2019
dbSNP: rs2221903
rs2221903
0.752 0.360 4 122617757 intron variant C/T snv 0.77
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma
0.010 1.000 1 2014 2014
dbSNP: rs2221903
rs2221903
0.752 0.360 4 122617757 intron variant C/T snv 0.77
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.010 1.000 1 2014 2014
dbSNP: rs2221903
rs2221903
0.752 0.360 4 122617757 intron variant C/T snv 0.77
CUI: C0007115
Disease: Malignant neoplasm of thyroid
Malignant neoplasm of thyroid
0.010 1.000 1 2014 2014
dbSNP: rs2221903
rs2221903
0.752 0.360 4 122617757 intron variant C/T snv 0.77
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs2221903
rs2221903
0.752 0.360 4 122617757 intron variant C/T snv 0.77
CUI: C0151517
Disease: Complete atrioventricular block
Complete atrioventricular block
0.010 1.000 1 2018 2018
dbSNP: rs2221903
rs2221903
0.752 0.360 4 122617757 intron variant C/T snv 0.77
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.010 < 0.001 1 2015 2015