rs920778, HOTAIR

N. diseases: 36
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.
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.030 1.000 3 2016 2018
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.030 1.000 3 2016 2018
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.030 1.000 3 2016 2018
Secondary malignant neoplasm of lymph node
188 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.030 1.000 3 2017 2019
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.040 0.750 4 2015 2018
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.040 0.750 4 2015 2018
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.040 1.000 4 2015 2020
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.040 1.000 4 2015 2017
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.040 1.000 4 2015 2020
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.100 0.938 16 2015 2020
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.100 0.938 16 2015 2020