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.
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
635 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.010 1 2017 2017
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
Malignant Head and Neck Neoplasm
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
117 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.010 1.000 1 2017 2017
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
169 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.010 1.000 1 2020 2020
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
861 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.010 1 2018 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
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
193 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.010 1.000 1 2016 2016
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
858 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.010 1 2018 2018
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
197 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.010 1.000 1 2018 2018
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
320 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.010 1.000 1 2014 2014
Uterine Fibroids
CUI: C0042133
Disease: Uterine Fibroids
52 0.633 0.480 12 53966448 intron variant G/A snv 0.57 0.010 1.000 1 2019 2019