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.
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.776 0.200 11 122152479 intron variant A/G snv 0.49 0.020 1.000 2 2014 2015
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.776 0.200 11 122152479 intron variant A/G snv 0.49 0.010 1 2018 2018
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.776 0.200 11 122152479 intron variant A/G snv 0.49 0.010 1.000 1 2014 2014
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.776 0.200 11 122152479 intron variant A/G snv 0.49 0.010 1.000 1 2014 2014
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.776 0.200 11 122152479 intron variant A/G snv 0.49 0.010 1.000 1 2016 2016
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.776 0.200 11 122152479 intron variant A/G snv 0.49 0.010 1.000 1 2019 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.776 0.200 11 122152479 intron variant A/G snv 0.49 0.010 1 2018 2018
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.776 0.200 11 122152479 intron variant A/G snv 0.49 0.010 1.000 1 2014 2014
Pain
CUI: C0030193
Disease: Pain
196 0.776 0.200 11 122152479 intron variant A/G snv 0.49 0.010 1.000 1 2016 2016