Source: BEFREE

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: rs11515
rs11515
0.882 0.040 9 21968200 3 prime UTR variant C/A;G snv 4.0E-06; 0.88
CUI: C3887461
Disease: Head and Neck Carcinoma
Head and Neck Carcinoma
0.010 < 0.001 1 2014 2014
dbSNP: rs11515
rs11515
0.882 0.040 9 21968200 3 prime UTR variant C/A;G snv 4.0E-06; 0.88
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2017 2017
dbSNP: rs11515
rs11515
0.882 0.040 9 21968200 3 prime UTR variant C/A;G snv 4.0E-06; 0.88
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2014 2014
dbSNP: rs11515
rs11515
0.882 0.040 9 21968200 3 prime UTR variant C/A;G snv 4.0E-06; 0.88
Squamous cell carcinoma of the head and neck
0.010 < 0.001 1 2014 2014
dbSNP: rs11515
rs11515
0.882 0.040 9 21968200 3 prime UTR variant C/A;G snv 4.0E-06; 0.88
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2017 2017
dbSNP: rs11515
rs11515
0.882 0.040 9 21968200 3 prime UTR variant C/A;G snv 4.0E-06; 0.88
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.010 1.000 1 2011 2011
dbSNP: rs3731249
rs3731249
0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02
CUI: C0025202
Disease: melanoma
melanoma
0.060 0.667 6 2002 2011
dbSNP: rs3731249
rs3731249
0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02
Childhood Acute Lymphoblastic Leukemia
0.030 1.000 3 2015 2018
dbSNP: rs3731249
rs3731249
0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.030 1.000 3 1998 2019
dbSNP: rs3731249
rs3731249
0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia
0.030 1.000 3 2015 2018
dbSNP: rs3731249
rs3731249
0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.030 0.667 3 2005 2007
dbSNP: rs3731249
rs3731249
0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.030 0.667 3 2005 2007
dbSNP: rs3731249
rs3731249
0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.020 1.000 2 2007 2009
dbSNP: rs3731249
rs3731249
0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.020 1.000 2 2007 2009
dbSNP: rs3731249
rs3731249
0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02
Meningioma, benign, no ICD-O subtype
0.010 1.000 1 2019 2019
dbSNP: rs3731249
rs3731249
0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02
CUI: C0025286
Disease: Meningioma
Meningioma
0.010 1.000 1 2019 2019
dbSNP: rs3731249
rs3731249
0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 1.000 1 2006 2006
dbSNP: rs3731249
rs3731249
0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 1.000 1 2006 2006
dbSNP: rs3731249
rs3731249
0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma
0.010 1.000 1 2011 2011
dbSNP: rs3731249
rs3731249
0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02
CUI: C0205748
Disease: Dysplastic Nevus
Dysplastic Nevus
0.010 1.000 1 2002 2002
dbSNP: rs3731249
rs3731249
0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02
CUI: C0027962
Disease: Melanocytic nevus
Melanocytic nevus
0.010 < 0.001 1 2002 2002
dbSNP: rs3731249
rs3731249
0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02
CUI: C0278877
Disease: Adult Meningioma
Adult Meningioma
0.010 1.000 1 2019 2019
dbSNP: rs3731249
rs3731249
0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02
CUI: C0027960
Disease: Nevus
Nevus
0.010 < 0.001 1 2002 2002
dbSNP: rs3731249
rs3731249
0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.010 1.000 1 2006 2006
dbSNP: rs3731249
rs3731249
0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02
CUI: C0334037
Disease: Intestinal metaplasia
Intestinal metaplasia
0.010 1.000 1 2012 2012