rs11969064, None

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.
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 6 18104864 intergenic variant C/T snv 0.11 0.700 1.000 1 2019 2019
Myelosuppression
CUI: C0854467
Disease: Myelosuppression
1 6 18104864 intergenic variant C/T snv 0.11 0.700 1.000 1 2019 2019