rs6774494, MECOM

N. diseases: 4
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.
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.882 0.160 3 169364845 intron variant G/A snv 0.42 0.740 1.000 5 2010 2017
Nasopharyngeal Neoplasms
CUI: C0027439
Disease: Nasopharyngeal Neoplasms
36 0.882 0.160 3 169364845 intron variant G/A snv 0.42 0.700 1.000 2 2010 2016
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.882 0.160 3 169364845 intron variant G/A snv 0.42 0.010 1.000 1 2014 2014
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.882 0.160 3 169364845 intron variant G/A snv 0.42 0.010 1.000 1 2014 2014