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: rs10828317
rs10828317
0.776 0.280 10 22550699 missense variant T/C snv
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 2 2013 2018
dbSNP: rs11013046
rs11013046
1.000 0.120 10 22551654 intron variant C/T snv 0.55
Precursor Cell Lymphoblastic Leukemia Lymphoma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2013 2013
dbSNP: rs370356098
rs370356098
1.000 0.080 10 22681806 intron variant G/C;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs4748813
rs4748813
1.000 0.120 10 22557806 intron variant T/A;C snv
Precursor Cell Lymphoblastic Leukemia Lymphoma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2018 2018
dbSNP: rs56333866
rs56333866
1.000 0.080 10 22581150 intron variant TTTC/- delins 0.97
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs7075634
rs7075634
1.000 0.120 10 22564173 intron variant T/C snv 0.57
Precursor Cell Lymphoblastic Leukemia Lymphoma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2013 2013
dbSNP: rs7081744
rs7081744
10 22558964 intron variant A/G snv 0.53
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs7088318
rs7088318
0.851 0.120 10 22564019 intron variant C/A snv 0.55
Precursor Cell Lymphoblastic Leukemia Lymphoma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2013 2013
dbSNP: rs7901152
rs7901152
1.000 0.120 10 22544224 intron variant G/A snv 0.66
Precursor Cell Lymphoblastic Leukemia Lymphoma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2013 2013
dbSNP: rs7904655
rs7904655
1.000 0.080 10 22549797 intron variant C/T snv 1.6E-02
Influenza due to Influenza A virus subtype H1N1
Infections; Respiratory Tract Diseases 0.700 1.000 1 2015 2015
dbSNP: rs7088318
rs7088318
0.851 0.120 10 22564019 intron variant C/A snv 0.55
Childhood Acute Lymphoblastic Leukemia
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.030 0.667 3 2013 2016
dbSNP: rs2230469
rs2230469
0.882 0.160 10 22550699 missense variant T/C snv 0.27 0.24
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.020 1.000 2 2008 2009
dbSNP: rs7088318
rs7088318
0.851 0.120 10 22564019 intron variant C/A snv 0.55
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia
0.020 1.000 2 2013 2016
dbSNP: rs7088318
rs7088318
0.851 0.120 10 22564019 intron variant C/A snv 0.55
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.020 1.000 2 2013 2016
dbSNP: rs10764338
rs10764338
1.000 10 22577963 intron variant T/C snv 0.82
Hyperdiploid B Acute Lymphoblastic Leukemia
0.010 1.000 1 2015 2015
dbSNP: rs10828317
rs10828317
0.776 0.280 10 22550699 missense variant T/C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs10828317
rs10828317
0.776 0.280 10 22550699 missense variant T/C snv
Hyperdiploid B Acute Lymphoblastic Leukemia
0.010 1.000 1 2013 2013
dbSNP: rs10828317
rs10828317
0.776 0.280 10 22550699 missense variant T/C snv
CUI: C0686347
Disease: Tardive Dyskinesia
Tardive Dyskinesia
Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.010 < 0.001 1 2014 2014
dbSNP: rs10828317
rs10828317
0.776 0.280 10 22550699 missense variant T/C snv
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2013 2013
dbSNP: rs10828317
rs10828317
0.776 0.280 10 22550699 missense variant T/C snv
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia
0.010 1.000 1 2013 2013
dbSNP: rs10828317
rs10828317
0.776 0.280 10 22550699 missense variant T/C snv
CUI: C3714760
Disease: Drug-induced tardive dyskinesia
Drug-induced tardive dyskinesia
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Chemically-Induced Disorders 0.010 < 0.001 1 2014 2014
dbSNP: rs10828317
rs10828317
0.776 0.280 10 22550699 missense variant T/C snv
Childhood Acute Lymphoblastic Leukemia
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2013 2013
dbSNP: rs10828317
rs10828317
0.776 0.280 10 22550699 missense variant T/C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2007 2007
dbSNP: rs11013052
rs11013052
1.000 0.040 10 22573558 intron variant C/A snv 0.27
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2008 2008
dbSNP: rs1409395
rs1409395
1.000 0.040 10 22643562 intron variant T/A;C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2010 2010