rs12508721, IL21-AS1

N. diseases: 11
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.742 0.360 4 122623509 intron variant C/T snv 0.24 0.010 1.000 1 2013 2013
Complete atrioventricular block
CUI: C0151517
Disease: Complete atrioventricular block
96 0.742 0.360 4 122623509 intron variant C/T snv 0.24 0.010 1.000 1 2017 2017
Cryptorchidism
CUI: C0010417
Disease: Cryptorchidism
80 0.742 0.360 4 122623509 intron variant C/T snv 0.24 0.010 1.000 1 2016 2016
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.742 0.360 4 122623509 intron variant C/T snv 0.24 0.010 1.000 1 2016 2016
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.742 0.360 4 122623509 intron variant C/T snv 0.24 0.010 1.000 1 2016 2016
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.742 0.360 4 122623509 intron variant C/T snv 0.24 0.010 1.000 1 2013 2013
Malignant neoplasm of thyroid
CUI: C0007115
Disease: Malignant neoplasm of thyroid
103 0.742 0.360 4 122623509 intron variant C/T snv 0.24 0.010 1.000 1 2014 2014
Sepsis
CUI: C0243026
Disease: Sepsis
144 0.742 0.360 4 122623509 intron variant C/T snv 0.24 0.010 1.000 1 2017 2017
Septicemia
CUI: C0036690
Disease: Septicemia
141 0.742 0.360 4 122623509 intron variant C/T snv 0.24 0.010 1.000 1 2017 2017
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.742 0.360 4 122623509 intron variant C/T snv 0.24 0.010 1.000 1 2014 2014
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.742 0.360 4 122623509 intron variant C/T snv 0.24 0.010 1.000 1 2014 2014