rs920778, HOTAIR

N. diseases: 36
Source: BEFREE ×
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.
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1441 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
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2145 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
2154 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
603 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
1571 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
616 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.040 1.000 4 2015 2020
cervical cancer
CUI: C4048328
Disease: cervical cancer
257 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
266 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
CUI: C0686619
Disease: 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
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
995 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.020 1.000 2 2018 2018
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
321 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.020 1.000 2 2017 2018
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
769 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.020 1.000 2 2017 2020
Malignant neoplasm of gastrointestinal tract
CUI: C0685938
Disease: Malignant neoplasm of gastrointestinal tract
55 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.020 1.000 2 2016 2017
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1000 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.020 1.000 2 2018 2018
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
246 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.020 1.000 2 2017 2018
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
229 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.020 1.000 2 2017 2018
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.020 1.000 2 2018 2018
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.010 1 2015 2015
Extrapulmonary Small Cell Carcinoma
CUI: C4722419
Disease: Extrapulmonary Small Cell Carcinoma
11 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.010 1.000 1 2014 2014
Familial lichen amyloidosis
CUI: C0268398
Disease: Familial lichen amyloidosis
24 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.010 1.000 1 2018 2018
Glioma
CUI: C0017638
Disease: Glioma
283 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.010 1 2017 2017
Head and Neck Carcinoma
CUI: C3887461
Disease: Head and Neck Carcinoma
118 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.010 1.000 1 2017 2017
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
269 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.010 1.000 1 2017 2017