rs3774937, NFKB1

N. diseases: 9
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.
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.776 0.280 4 102513096 intron variant T/C snv 0.26 0.700 1.000 2 2015 2016
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.776 0.280 4 102513096 intron variant T/C snv 0.26 0.700 1.000 1 2016 2016
Cholangitis, Sclerosing
CUI: C0008313
Disease: Cholangitis, Sclerosing
276 0.776 0.280 4 102513096 intron variant T/C snv 0.26 0.700 1.000 1 2016 2016
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.776 0.280 4 102513096 intron variant T/C snv 0.26 0.700 1.000 1 2016 2016
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.776 0.280 4 102513096 intron variant T/C snv 0.26 0.700 1.000 1 2016 2016
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.776 0.280 4 102513096 intron variant T/C snv 0.26 0.010 1.000 1 2019 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.776 0.280 4 102513096 intron variant T/C snv 0.26 0.010 1.000 1 2019 2019
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.776 0.280 4 102513096 intron variant T/C snv 0.26 0.010 1.000 1 2019 2019
Sensorineural Hearing Loss (disorder)
111 0.776 0.280 4 102513096 intron variant T/C snv 0.26 0.010 1.000 1 2014 2014