rs2073643, SLC22A5

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.
Asthma
CUI: C0004096
Disease: Asthma
1536 1.000 0.080 5 132387596 intron variant T/C snv 0.46 0.800 1.000 3 2010 2012
fibrinogen activity
CUI: C1325327
Disease: fibrinogen activity
63 1.000 0.080 5 132387596 intron variant T/C snv 0.46 0.700 1.000 1 2011 2011
Fibrinogen assay
CUI: C0337428
Disease: Fibrinogen assay
143 1.000 0.080 5 132387596 intron variant T/C snv 0.46 0.700 1.000 1 2011 2011
Fibrinogen, CTCAE
CUI: C1561955
Disease: Fibrinogen, CTCAE
63 1.000 0.080 5 132387596 intron variant T/C snv 0.46 0.700 1.000 1 2011 2011