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.
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.677 0.400 5 168768351 intron variant G/A snv 0.25 0.040 1.000 4 2010 2017
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.677 0.400 5 168768351 intron variant G/A snv 0.25 0.040 0.750 4 2014 2018
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.677 0.400 5 168768351 intron variant G/A snv 0.25 0.040 0.750 4 2014 2018
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.677 0.400 5 168768351 intron variant G/A snv 0.25 0.030 1.000 3 2010 2017
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.677 0.400 5 168768351 intron variant G/A snv 0.25 0.030 0.667 3 2012 2014
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.677 0.400 5 168768351 intron variant G/A snv 0.25 0.030 1.000 3 2010 2017
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.677 0.400 5 168768351 intron variant G/A snv 0.25 0.020 1.000 2 2014 2018
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.677 0.400 5 168768351 intron variant G/A snv 0.25 0.010 1.000 1 2018 2018
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.677 0.400 5 168768351 intron variant G/A snv 0.25 0.010 1.000 1 2018 2018
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.677 0.400 5 168768351 intron variant G/A snv 0.25 0.010 1.000 1 2013 2013
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
231 0.677 0.400 5 168768351 intron variant G/A snv 0.25 0.010 1.000 1 2018 2018
Cervical Intraepithelial Neoplasia
CUI: C0206708
Disease: Cervical Intraepithelial Neoplasia
29 0.677 0.400 5 168768351 intron variant G/A snv 0.25 0.010 1.000 1 2017 2017
Childhood Neuroblastoma
CUI: C4086165
Disease: Childhood Neuroblastoma
231 0.677 0.400 5 168768351 intron variant G/A snv 0.25 0.010 1.000 1 2018 2018
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.677 0.400 5 168768351 intron variant G/A snv 0.25 0.010 1 2013 2013
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.677 0.400 5 168768351 intron variant G/A snv 0.25 0.010 1.000 1 2014 2014
Hepatocarcinogenesis
CUI: C1512409
Disease: Hepatocarcinogenesis
24 0.677 0.400 5 168768351 intron variant G/A snv 0.25 0.010 1.000 1 2014 2014
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.677 0.400 5 168768351 intron variant G/A snv 0.25 0.010 1.000 1 2018 2018
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.677 0.400 5 168768351 intron variant G/A snv 0.25 0.010 1.000 1 2017 2017
Mucocutaneous Lymph Node Syndrome
CUI: C0026691
Disease: Mucocutaneous Lymph Node Syndrome
195 0.677 0.400 5 168768351 intron variant G/A snv 0.25 0.010 1 2018 2018
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.677 0.400 5 168768351 intron variant G/A snv 0.25 0.010 1.000 1 2014 2014
Neuroblastoma
CUI: C0027819
Disease: Neuroblastoma
386 0.677 0.400 5 168768351 intron variant G/A snv 0.25 0.010 1.000 1 2018 2018
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.677 0.400 5 168768351 intron variant G/A snv 0.25 0.010 1.000 1 2018 2018
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.677 0.400 5 168768351 intron variant G/A snv 0.25 0.010 1.000 1 2018 2018
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.677 0.400 5 168768351 intron variant G/A snv 0.25 0.010 1.000 1 2017 2017