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.
Malignant Female Reproductive System Neoplasm
CUI: C0699889
Disease: Malignant Female Reproductive System Neoplasm
5 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.010 1.000 1 2019 2019
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
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
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
Malignant Head and Neck Neoplasm
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
118 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.010 1.000 1 2017 2017
Uterine Fibroids
CUI: C0042133
Disease: Uterine Fibroids
154 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.010 1.000 1 2019 2019
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
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.010 1.000 1 2016 2016
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.010 1.000 1 2020 2020
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
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.010 1.000 1 2018 2018
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 neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
315 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.020 1.000 2 2017 2018
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.020 1.000 2 2017 2018
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.010 1.000 1 2016 2016
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.010 1.000 1 2014 2014
Glioma
CUI: C0017638
Disease: Glioma
353 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.010 1 2017 2017
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.010 1 2015 2015
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.010 1.000 1 2017 2017
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
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
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 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
942 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.020 1.000 2 2017 2020