rs1074182, RBL2

N. diseases: 2
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.
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 1.000 0.080 16 53437445 intron variant T/G snv 0.55 0.010 1.000 1 2009 2009
Retinoblastoma
CUI: C0035335
Disease: Retinoblastoma
193 1.000 0.080 16 53437445 intron variant T/G snv 0.55 0.010 1.000 1 2009 2009