rs9001, CHDH

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.
Choline Deficiency
CUI: C0008412
Disease: Choline Deficiency
4 0.925 0.080 3 53823890 missense variant T/G snv 0.15 0.17 0.010 1.000 1 2006 2006
Hyperhomocysteinemia
CUI: C0598608
Disease: Hyperhomocysteinemia
45 0.925 0.080 3 53823890 missense variant T/G snv 0.15 0.17 0.010 1.000 1 2009 2009