Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10512597
rs10512597
17 74703694 intron variant T/A;C snv
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.800 1.000 3 2009 2017
dbSNP: rs10512597
rs10512597
17 74703694 intron variant T/A;C snv
CUI: C1561955
Disease: Fibrinogen, CTCAE
Fibrinogen, CTCAE
0.700 1.000 2 2009 2013
dbSNP: rs10512597
rs10512597
17 74703694 intron variant T/A;C snv
CUI: C1325327
Disease: fibrinogen activity
fibrinogen activity
0.700 1.000 2 2009 2013
dbSNP: rs1037171
rs1037171
17 74706839 intron variant G/A snv 0.53
CUI: C0750880
Disease: Monocyte count result
Monocyte count result
0.700 1.000 1 2016 2016
dbSNP: rs1037171
rs1037171
17 74706839 intron variant G/A snv 0.53
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs10512597
rs10512597
17 74703694 intron variant T/A;C snv
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2018 2018
dbSNP: rs2034310
rs2034310
17 74695789 missense variant T/C snv 0.77 0.74
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs2084312
rs2084312
17 74699072 intron variant C/A;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs2384955
rs2384955
17 74699028 intron variant T/C snv 0.69
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2018 2018
dbSNP: rs34074270
rs34074270
17 74706280 intron variant A/G;T snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2019 2019
dbSNP: rs35489971
rs35489971
1.000 0.040 17 74704804 missense variant A/G;T snv 0.73
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.700 1.000 1 2017 2017
dbSNP: rs35489971
rs35489971
1.000 0.040 17 74704804 missense variant A/G;T snv 0.73
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs749780
rs749780
17 74703245 intron variant C/A snv 0.54
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs749780
rs749780
17 74703245 intron variant C/A snv 0.54
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2016 2016
dbSNP: rs749780
rs749780
17 74703245 intron variant C/A snv 0.54
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs749780
rs749780
17 74703245 intron variant C/A snv 0.54
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
0.700 1.000 1 2016 2016
dbSNP: rs77936863
rs77936863
17 74700954 intron variant A/- del 0.54
CUI: C0857490
Disease: Granulocyte count
Granulocyte count
0.700 1.000 1 2016 2016
dbSNP: rs9903991
rs9903991
17 74705815 intron variant A/G snv 0.65
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2019 2019
dbSNP: rs141171369
rs141171369
1.000 0.080 17 74704762 missense variant C/T snv 2.2E-04 1.3E-04
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
Immune System Diseases; Nervous System Diseases 0.010 1.000 1 2017 2017