rs2158177, TH2LCRR

N. diseases: 5
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.
Dermatitis, Atopic
CUI: C0011615
Disease: Dermatitis, Atopic
232 0.925 0.120 5 132648366 intron variant A/G snv 0.18 0.710 1.000 2 2013 2017
fibrinogen activity
CUI: C1325327
Disease: fibrinogen activity
63 0.925 0.120 5 132648366 intron variant A/G snv 0.18 0.700 1.000 1 2011 2011
Fibrinogen assay
CUI: C0337428
Disease: Fibrinogen assay
143 0.925 0.120 5 132648366 intron variant A/G snv 0.18 0.700 1.000 1 2011 2011
Fibrinogen, CTCAE
CUI: C1561955
Disease: Fibrinogen, CTCAE
63 0.925 0.120 5 132648366 intron variant A/G snv 0.18 0.700 1.000 1 2011 2011
Eczema
CUI: C0013595
Disease: Eczema
368 0.925 0.120 5 132648366 intron variant A/G snv 0.18 0.010 1.000 1 2017 2017