rs796065343, CSF3R

N. diseases: 12
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.
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.776 0.080 1 36467833 missense variant G/A snv 0.700 1.000 1 2013 2013
Myeloid Leukemia, Chronic
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
115 0.776 0.080 1 36467833 missense variant G/A snv 0.700 1.000 1 2013 2013
Chronic Neutrophilic Leukemia
CUI: C0023481
Disease: Chronic Neutrophilic Leukemia
4 0.776 0.080 1 36467833 missense variant G/A snv 0.070 1.000 7 2013 2020
Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative
CUI: C1292772
Disease: Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative
5 0.776 0.080 1 36467833 missense variant G/A snv 0.050 1.000 5 2014 2020
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.776 0.080 1 36467833 missense variant G/A snv 0.010 1.000 1 2018 2018
Chronic myeloproliferative disorder
CUI: C1292778
Disease: Chronic myeloproliferative disorder
47 0.776 0.080 1 36467833 missense variant G/A snv 0.010 1.000 1 2013 2013
leukemia
CUI: C0023418
Disease: leukemia
144 0.776 0.080 1 36467833 missense variant G/A snv 0.010 1.000 1 2018 2018
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.776 0.080 1 36467833 missense variant G/A snv 0.010 1.000 1 2016 2016
Myeloproliferative disease
CUI: C0027022
Disease: Myeloproliferative disease
43 0.776 0.080 1 36467833 missense variant G/A snv 0.010 1.000 1 2013 2013
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.776 0.080 1 36467833 missense variant G/A snv 0.010 1.000 1 2013 2013
Neutrophilic Leukemia
CUI: C0474856
Disease: Neutrophilic Leukemia
2 0.776 0.080 1 36467833 missense variant G/A snv 0.010 1.000 1 2018 2018
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.776 0.080 1 36467833 missense variant G/A snv 0.010 1.000 1 2016 2016