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: rs2231142
rs2231142
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12
CUI: C0018099
Disease: Gout
Gout
0.820 1.000 2 2008 2019
dbSNP: rs2231142
rs2231142
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.810 1.000 1 2008 2019
dbSNP: rs2231142
rs2231142
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12
CUI: C0740394
Disease: Hyperuricemia
Hyperuricemia
0.800 1.000 10 2010 2019
dbSNP: rs2231142
rs2231142
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.040 1.000 4 2005 2019
dbSNP: rs2231142
rs2231142
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.040 1.000 4 2005 2019
dbSNP: rs2231142
rs2231142
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
Myeloid Leukemia, Chronic
0.040 1.000 4 2013 2018
dbSNP: rs2231137
rs2231137
0.752 0.400 4 88139962 missense variant C/T snv 0.11 7.4E-02
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
Diffuse Large B-Cell Lymphoma
0.030 1.000 3 2007 2017
dbSNP: rs2231142
rs2231142
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.030 1.000 3 2007 2016
dbSNP: rs2231142
rs2231142
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12
CUI: C0011991
Disease: Diarrhea
Diarrhea
0.030 1.000 3 2006 2019
dbSNP: rs2231142
rs2231142
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.030 1.000 3 2013 2019
dbSNP: rs2231137
rs2231137
0.752 0.400 4 88139962 missense variant C/T snv 0.11 7.4E-02
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.020 1.000 2 2009 2018
dbSNP: rs2231142
rs2231142
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.020 0.500 2 2008 2017
dbSNP: rs2231142
rs2231142
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.020 0.500 2 2008 2017
dbSNP: rs2231142
rs2231142
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
Diffuse Large B-Cell Lymphoma
0.020 1.000 2 2007 2008
dbSNP: rs2231142
rs2231142
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.020 1.000 2 2007 2016
dbSNP: rs2231142
rs2231142
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12
CUI: C0014544
Disease: Epilepsy
Epilepsy
0.020 1.000 2 2016 2018
dbSNP: rs2231142
rs2231142
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.020 1.000 2 2005 2019
dbSNP: rs10011796
rs10011796
0.882 0.160 4 88169725 intron variant T/C;G snv
CUI: C0221248
Disease: Tophus
Tophus
0.010 1.000 1 2017 2017
dbSNP: rs1185675198
rs1185675198
0.925 0.080 4 88121789 missense variant C/T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 < 0.001 1 2011 2011
dbSNP: rs1185675198
rs1185675198
0.925 0.080 4 88121789 missense variant C/T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 < 0.001 1 2011 2011
dbSNP: rs1305398818
rs1305398818
0.925 0.080 4 88131886 missense variant G/A;C snv 4.0E-06; 4.0E-06
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs1305398818
rs1305398818
0.925 0.080 4 88131886 missense variant G/A;C snv 4.0E-06; 4.0E-06
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.010 1.000 1 2013 2013
dbSNP: rs1305398818
rs1305398818
0.925 0.080 4 88131886 missense variant G/A;C snv 4.0E-06; 4.0E-06
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2013 2013
dbSNP: rs1305398818
rs1305398818
0.925 0.080 4 88131886 missense variant G/A;C snv 4.0E-06; 4.0E-06
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2013 2013
dbSNP: rs1481012
rs1481012
0.882 0.200 4 88117930 intron variant A/G snv 8.9E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2008 2008