rs4846913, GALNT2

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.
RDW - Red blood cell distribution width result
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
988 1.000 0.120 1 230158968 intron variant C/A;T snv 0.700 1.000 1 2019 2019
Red cell distribution width determination
CUI: C0427460
Disease: Red cell distribution width determination
988 1.000 0.120 1 230158968 intron variant C/A;T snv 0.700 1.000 1 2019 2019
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 1.000 0.120 1 230158968 intron variant C/A;T snv 0.010 1.000 1 2016 2016
Hypochondroplasia (disorder)
CUI: C0410529
Disease: Hypochondroplasia (disorder)
42 1.000 0.120 1 230158968 intron variant C/A;T snv 0.010 1.000 1 2016 2016