rs3731217, CDKN2A

N. diseases: 10
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.
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
CUI: C0023485
Disease: Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
21 0.763 0.320 9 21984662 intron variant A/C;T snv 0.700 1.000 2 2013 2018
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.763 0.320 9 21984662 intron variant A/C;T snv 0.050 1.000 5 2010 2018
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.763 0.320 9 21984662 intron variant A/C;T snv 0.030 1.000 3 2010 2018
Adult Acute Lymphocytic Leukemia
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
154 0.763 0.320 9 21984662 intron variant A/C;T snv 0.020 1.000 2 2017 2018
Differentiated Thyroid Gland Carcinoma
CUI: C1337013
Disease: Differentiated Thyroid Gland Carcinoma
80 0.763 0.320 9 21984662 intron variant A/C;T snv 0.010 1.000 1 2013 2013
Hyperdiploid B Acute Lymphoblastic Leukemia
CUI: C2697636
Disease: Hyperdiploid B Acute Lymphoblastic Leukemia
13 0.763 0.320 9 21984662 intron variant A/C;T snv 0.010 1.000 1 2015 2015
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.763 0.320 9 21984662 intron variant A/C;T snv 0.010 1.000 1 2014 2014
Precursor Cell Lymphoblastic Leukemia Lymphoma
CUI: C1961102
Disease: Precursor Cell Lymphoblastic Leukemia Lymphoma
168 0.763 0.320 9 21984662 intron variant A/C;T snv 0.010 1.000 1 2010 2010
SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT
CUI: C2678061
Disease: SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT
12 0.763 0.320 9 21984662 intron variant A/C;T snv 0.010 1.000 1 2011 2011
Squamous cell carcinoma of oropharynx
CUI: C0280313
Disease: Squamous cell carcinoma of oropharynx
33 0.763 0.320 9 21984662 intron variant A/C;T snv 0.010 1.000 1 2014 2014