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: rs376373278
rs376373278
MPO
0.882 0.120 17 58279015 missense variant G/A;C snv 4.2E-06
CUI: C1623038
Disease: Cirrhosis
Cirrhosis
0.020 1.000 2 2011 2012
dbSNP: rs376373278
rs376373278
MPO
0.882 0.120 17 58279015 missense variant G/A;C snv 4.2E-06
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis
0.020 1.000 2 2011 2012
dbSNP: rs972427414
rs972427414
MPO
0.882 0.120 17 58279379 missense variant A/G snv
CUI: C1623038
Disease: Cirrhosis
Cirrhosis
0.020 1.000 2 2011 2012
dbSNP: rs972427414
rs972427414
MPO
0.882 0.120 17 58279379 missense variant A/G snv
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis
0.020 1.000 2 2011 2012
dbSNP: rs1207692596
rs1207692596
MPO
0.925 0.080 17 58280438 missense variant G/A;T snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 < 0.001 1 2013 2013
dbSNP: rs1207692596
rs1207692596
MPO
0.925 0.080 17 58280438 missense variant G/A;T snv
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.010 1.000 1 2013 2013
dbSNP: rs1207692596
rs1207692596
MPO
0.925 0.080 17 58280438 missense variant G/A;T snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 < 0.001 1 2013 2013
dbSNP: rs1271546630
rs1271546630
MPO
1.000 0.120 17 58277848 missense variant G/A;C snv
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth
0.010 1.000 1 2010 2010
dbSNP: rs1271546630
rs1271546630
MPO
1.000 0.120 17 58277848 missense variant G/A;C snv
CUI: C0151546
Disease: Oral Cavity Carcinoma
Oral Cavity Carcinoma
0.010 1.000 1 2010 2010
dbSNP: rs1351260902
rs1351260902
MPO
1.000 0.080 17 58279839 missense variant C/G;T snv
CUI: C0586354
Disease: Esophageal dysplasia
Esophageal dysplasia
0.010 1.000 1 2008 2008
dbSNP: rs2243828
rs2243828
MPO
0.925 0.080 17 58281523 upstream gene variant A/G;T snv
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.010 1.000 1 2012 2012
dbSNP: rs2243828
rs2243828
MPO
0.925 0.080 17 58281523 upstream gene variant A/G;T snv
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2012 2012
dbSNP: rs376373278
rs376373278
MPO
0.882 0.120 17 58279015 missense variant G/A;C snv 4.2E-06
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs7208693
rs7208693
MPO
0.882 0.080 17 58280457 missense variant C/A;T snv 9.0E-02
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 1.000 1 2014 2014
dbSNP: rs7208693
rs7208693
MPO
0.882 0.080 17 58280457 missense variant C/A;T snv 9.0E-02
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.010 1.000 1 2014 2014
dbSNP: rs7208693
rs7208693
MPO
0.882 0.080 17 58280457 missense variant C/A;T snv 9.0E-02
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 1.000 1 2014 2014
dbSNP: rs7208693
rs7208693
MPO
0.882 0.080 17 58280457 missense variant C/A;T snv 9.0E-02
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.010 1.000 1 2006 2006
dbSNP: rs8082134
rs8082134
MPO
0.925 0.080 17 58275265 intron variant G/A;T snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 1.000 1 2012 2012
dbSNP: rs8082134
rs8082134
MPO
0.925 0.080 17 58275265 intron variant G/A;T snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 1.000 1 2012 2012
dbSNP: rs972427414
rs972427414
MPO
0.882 0.120 17 58279379 missense variant A/G snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs119469012
rs119469012
MPO
1.000 0.080 17 58272825 missense variant A/C;G snv
CUI: C0398595
Disease: Myeloperoxidase Deficiency
Myeloperoxidase Deficiency
0.700 0
dbSNP: rs119469013
rs119469013
MPO
1.000 0.080 17 58273534 missense variant C/A;T snv 4.0E-06
CUI: C0398595
Disease: Myeloperoxidase Deficiency
Myeloperoxidase Deficiency
0.700 0
dbSNP: rs119469014
rs119469014
MPO
1.000 0.080 17 58273540 missense variant G/A;C snv 2.4E-05; 2.0E-05
CUI: C0398595
Disease: Myeloperoxidase Deficiency
Myeloperoxidase Deficiency
0.700 0
dbSNP: rs767523236
rs767523236
MPO
0.925 0.040 17 58279033 missense variant T/C snv 4.1E-06 7.0E-06
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
0.010 1.000 1 2009 2009
dbSNP: rs767523236
rs767523236
MPO
0.925 0.040 17 58279033 missense variant T/C snv 4.1E-06 7.0E-06
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.010 1.000 1 2009 2009