Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12573787
rs12573787
1.000 0.080 10 87863959 5 prime UTR variant G/A;C snv
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
Myeloid Leukemia, Chronic
0.010 1.000 1 2019 2019
dbSNP: rs1205454520
rs1205454520
0.763 0.120 10 87864059 5 prime UTR variant -/G delins 7.2E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.030 1.000 3 2001 2015
dbSNP: rs1205454520
rs1205454520
0.763 0.120 10 87864059 5 prime UTR variant -/G delins 7.2E-06
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.010 1.000 1 2001 2001
dbSNP: rs1205454520
rs1205454520
0.763 0.120 10 87864059 5 prime UTR variant -/G delins 7.2E-06
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
0.010 < 0.001 1 2007 2007
dbSNP: rs1205454520
rs1205454520
0.763 0.120 10 87864059 5 prime UTR variant -/G delins 7.2E-06
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.010 < 0.001 1 2007 2007
dbSNP: rs1205454520
rs1205454520
0.763 0.120 10 87864059 5 prime UTR variant -/G delins 7.2E-06
CUI: C0278878
Disease: Adult Glioblastoma
Adult Glioblastoma
0.010 < 0.001 1 2007 2007
dbSNP: rs1205454520
rs1205454520
0.763 0.120 10 87864059 5 prime UTR variant -/G delins 7.2E-06
CUI: C0280474
Disease: Childhood Glioblastoma
Childhood Glioblastoma
0.010 < 0.001 1 2007 2007
dbSNP: rs1205454520
rs1205454520
0.763 0.120 10 87864059 5 prime UTR variant -/G delins 7.2E-06
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 1.000 1 2016 2016
dbSNP: rs1205454520
rs1205454520
0.763 0.120 10 87864059 5 prime UTR variant -/G delins 7.2E-06
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 1.000 1 2016 2016
dbSNP: rs1205454520
rs1205454520
0.763 0.120 10 87864059 5 prime UTR variant -/G delins 7.2E-06
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.010 1.000 1 2016 2016
dbSNP: rs1205454520
rs1205454520
0.763 0.120 10 87864059 5 prime UTR variant -/G delins 7.2E-06
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2001 2001
dbSNP: rs1029342144
rs1029342144
0.882 0.120 10 87864162 5 prime UTR variant C/G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.020 0.500 2 2005 2011
dbSNP: rs1029342144
rs1029342144
0.882 0.120 10 87864162 5 prime UTR variant C/G;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs1029342144
rs1029342144
0.882 0.120 10 87864162 5 prime UTR variant C/G;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2005 2005
dbSNP: rs1029342144
rs1029342144
0.882 0.120 10 87864162 5 prime UTR variant C/G;T snv
Squamous cell carcinoma of esophagus
0.010 1.000 1 2012 2012
dbSNP: rs1029342144
rs1029342144
0.882 0.120 10 87864162 5 prime UTR variant C/G;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2005 2005
dbSNP: rs1029342144
rs1029342144
0.882 0.120 10 87864162 5 prime UTR variant C/G;T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2011 2011
dbSNP: rs1239105602
rs1239105602
1.000 0.160 10 87864168 5 prime UTR variant C/T snv
CUI: C0376545
Disease: Hematologic Neoplasms
Hematologic Neoplasms
0.010 1.000 1 2007 2007
dbSNP: rs1239105602
rs1239105602
1.000 0.160 10 87864168 5 prime UTR variant C/T snv
CUI: C0028326
Disease: Noonan Syndrome
Noonan Syndrome
0.010 1.000 1 2007 2007
dbSNP: rs917927904
rs917927904
1.000 0.160 10 87864242 5 prime UTR variant G/T snv 7.0E-06
CUI: C0028326
Disease: Noonan Syndrome
Noonan Syndrome
0.010 1.000 1 2007 2007
dbSNP: rs917927904
rs917927904
1.000 0.160 10 87864242 5 prime UTR variant G/T snv 7.0E-06
CUI: C0376545
Disease: Hematologic Neoplasms
Hematologic Neoplasms
0.010 1.000 1 2007 2007
dbSNP: rs1564801388
rs1564801388
1.000 0.040 10 87864353 5 prime UTR variant -/G delins
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
0.700 1.000 1 2019 2019
dbSNP: rs1564801473
rs1564801473
1.000 0.040 10 87864406 5 prime UTR variant -/C delins
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
0.700 1.000 1 2019 2019
dbSNP: rs11202592
rs11202592
0.851 0.200 10 87864461 5 prime UTR variant C/G snv 3.8E-03 1.4E-03
CUI: C0028754
Disease: Obesity
Obesity
0.010 1.000 1 2013 2013
dbSNP: rs11202592
rs11202592
0.851 0.200 10 87864461 5 prime UTR variant C/G snv 3.8E-03 1.4E-03
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.010 < 0.001 1 2013 2013