rs13254990, PVT1

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.
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.882 0.120 8 128064205 intron variant C/T snv 0.24 0.010 1.000 1 2019 2019
Lymphoma, Follicular
CUI: C0024301
Disease: Lymphoma, Follicular
83 0.882 0.120 8 128064205 intron variant C/T snv 0.24 0.010 1.000 1 2014 2014
Mature B-Cell Neoplasm
CUI: C1334633
Disease: Mature B-Cell Neoplasm
15 0.882 0.120 8 128064205 intron variant C/T snv 0.24 0.700 1.000 1 2014 2014
Non-Hodgkin's lymphoma of central nervous system
5 0.882 0.120 8 128064205 intron variant C/T snv 0.24 0.700 1.000 1 2019 2019