rs1672753, CRBN

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.
Constipation
CUI: C0009806
Disease: Constipation
57 0.882 0.240 3 3179746 upstream gene variant C/T snv 0.71 0.010 1.000 1 2019 2019
Hyperbilirubinemia
CUI: C0020433
Disease: Hyperbilirubinemia
27 0.882 0.240 3 3179746 upstream gene variant C/T snv 0.71 0.010 1 2019 2019
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.882 0.240 3 3179746 upstream gene variant C/T snv 0.71 0.010 1.000 1 2019 2019
Polyneuropathy
CUI: C0152025
Disease: Polyneuropathy
32 0.882 0.240 3 3179746 upstream gene variant C/T snv 0.71 0.010 1.000 1 2019 2019