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: 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: 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: rs2107545
rs2107545
MPO
0.925 0.160 17 58282757 upstream gene variant A/G snv 0.28
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.010 1.000 1 2017 2017
dbSNP: rs2107545
rs2107545
MPO
0.925 0.160 17 58282757 upstream gene variant A/G snv 0.28
Diabetes Mellitus, Non-Insulin-Dependent
0.010 1.000 1 2018 2018
dbSNP: rs376919235
rs376919235
MPO
1.000 0.080 17 58279366 synonymous variant A/G snv 1.4E-05 7.0E-06
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.010 1.000 1 2005 2005
dbSNP: rs56378716
rs56378716
MPO
1.000 0.080 17 58279141 missense variant A/G snv 1.0E-02 9.8E-03
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2016 2016
dbSNP: rs56378716
rs56378716
MPO
1.000 0.080 17 58279141 missense variant A/G snv 1.0E-02 9.8E-03
CUI: C0398595
Disease: Myeloperoxidase Deficiency
Myeloperoxidase Deficiency
0.810 1.000 1 1998 1998
dbSNP: rs56378716
rs56378716
MPO
1.000 0.080 17 58279141 missense variant A/G snv 1.0E-02 9.8E-03
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
0.700 1.000 1 2016 2016
dbSNP: rs56378716
rs56378716
MPO
1.000 0.080 17 58279141 missense variant A/G snv 1.0E-02 9.8E-03
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs56378716
rs56378716
MPO
1.000 0.080 17 58279141 missense variant A/G snv 1.0E-02 9.8E-03
CUI: C0857490
Disease: Granulocyte count
Granulocyte count
0.700 1.000 1 2016 2016
dbSNP: rs56378716
rs56378716
MPO
1.000 0.080 17 58279141 missense variant A/G snv 1.0E-02 9.8E-03
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
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: 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: 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: 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: 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: rs2333227
rs2333227
MPO
0.752 0.320 17 58281401 upstream gene variant C/T snv 0.24
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.030 1.000 3 2012 2018
dbSNP: rs2333227
rs2333227
MPO
0.752 0.320 17 58281401 upstream gene variant C/T snv 0.24
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.020 0.500 2 2008 2013
dbSNP: rs2333227
rs2333227
MPO
0.752 0.320 17 58281401 upstream gene variant C/T snv 0.24
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.020 1.000 2 2012 2018
dbSNP: rs2333227
rs2333227
MPO
0.752 0.320 17 58281401 upstream gene variant C/T snv 0.24
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.020 0.500 2 2008 2013