rs10489615, GALNT2

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.
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 1 230169242 intron variant A/C;G snv 0.800 1.000 1 2010 2010
Fibrinogen assay
CUI: C0337428
Disease: Fibrinogen assay
143 1 230169242 intron variant A/C;G snv 0.700 1.000 1 2017 2017
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 1 230169242 intron variant A/C;G snv 0.700 1.000 1 2010 2010