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. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Hypertensive disease
|
1085 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.840 | 1.000 | 5 | 2011 | 2019 | ||||
Hereditary hemochromatosis
|
56 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.800 | 0.991 | 114 | 1996 | 2019 | ||||
HEMOCHROMATOSIS, TYPE 1
|
62 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.800 | 0.960 | 99 | 1996 | 2019 | ||||
Alzheimer's Disease
|
1843 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.800 | 0.882 | 17 | 2003 | 2016 | ||||
Corpuscular Hemoglobin Concentration Mean
|
4389 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.800 | 1.000 | 3 | 2012 | 2018 | ||||
Hemoglobin measurement
|
224 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.800 | 1.000 | 2 | 2009 | 2016 | ||||
Cystic Fibrosis
|
704 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.720 | 1.000 | 2 | 2003 | 2010 | ||||
Variegate Porphyria
|
24 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.710 | 1.000 | 1 | 1999 | 1999 | ||||
Diastolic blood pressure
|
1037 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.700 | 1.000 | 6 | 2011 | 2018 | ||||
Systolic Pressure
|
1931 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.700 | 1.000 | 5 | 2011 | 2018 | ||||
Blood Pressure
|
220 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.700 | 1.000 | 2 | 2011 | 2011 | ||||
Serum iron measurement
|
25 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.700 | 1.000 | 2 | 2011 | 2017 | ||||
Diastolic blood pressure measurement
|
81 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||
Ferritin measurement
|
21 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
Finding of Mean Corpuscular Hemoglobin
|
1206 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||
Hematocrit procedure
|
216 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
Hemoglobin, CTCAE
|
26 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||
Iron level result
|
16 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||
Iron measurement
|
16 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||
Mean blood pressure
|
344 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
Platelet Count measurement
|
457 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
RDW - Red blood cell distribution width result
|
988 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
Red Blood Cell Count measurement
|
1599 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||
Red cell distribution width determination
|
988 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
Reticulocyte count (procedure)
|
474 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 0.700 | 1.000 | 1 | 2016 | 2016 |