rs12651106, DCHS2

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.
Fibrinogen assay
CUI: C0337428
Disease: Fibrinogen assay
143 4 154379907 intron variant C/A snv 0.12 0.800 1.000 1 2011 2011
fibrinogen activity
CUI: C1325327
Disease: fibrinogen activity
63 4 154379907 intron variant C/A snv 0.12 0.700 1.000 1 2011 2011
Fibrinogen, CTCAE
CUI: C1561955
Disease: Fibrinogen, CTCAE
63 4 154379907 intron variant C/A snv 0.12 0.700 1.000 1 2011 2011