rs10099100, None

N. diseases: 3
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.
Child Development Disorders, Pervasive
CUI: C0008074
Disease: Child Development Disorders, Pervasive
379 8 10719265 downstream gene variant G/C snv 0.32 0.700 1.000 1 2019 2019
RDW - Red blood cell distribution width result
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
988 8 10719265 downstream gene variant G/C snv 0.32 0.700 1.000 1 2019 2019
Red cell distribution width determination
CUI: C0427460
Disease: Red cell distribution width determination
988 8 10719265 downstream gene variant G/C snv 0.32 0.700 1.000 1 2019 2019