DAB2IP, DAB2 interacting protein, 153090

N. diseases: 74; N. variants: 4
Source: BEFREE ×
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7025486
rs7025486
0.851 0.040 9 121660124 intron variant G/A snv 0.28
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
Aortic Aneurysm, Abdominal
Cardiovascular Diseases 0.810 1.000 1 2010 2010
dbSNP: rs7025486
rs7025486
0.851 0.040 9 121660124 intron variant G/A snv 0.28
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.020 1.000 2 2012 2017
dbSNP: rs13290547
rs13290547
9 121725216 intron variant C/T snv 4.0E-02
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs1571801
rs1571801
0.827 0.120 9 121665094 intron variant G/T snv 0.21
CUI: C0033578
Disease: Prostatic Neoplasms
Prostatic Neoplasms
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2007 2007
dbSNP: rs1571801
rs1571801
0.827 0.120 9 121665094 intron variant G/T snv 0.21
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1571801
rs1571801
0.827 0.120 9 121665094 intron variant G/T snv 0.21
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1571801
rs1571801
0.827 0.120 9 121665094 intron variant G/T snv 0.21
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2007 2007
dbSNP: rs1571801
rs1571801
0.827 0.120 9 121665094 intron variant G/T snv 0.21
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1571801
rs1571801
0.827 0.120 9 121665094 intron variant G/T snv 0.21
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2007 2007
dbSNP: rs2243421
rs2243421
0.925 0.080 9 121631045 intron variant C/T snv 0.44
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs2243421
rs2243421
0.925 0.080 9 121631045 intron variant C/T snv 0.44
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs7025486
rs7025486
0.851 0.040 9 121660124 intron variant G/A snv 0.28
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs7025486
rs7025486
0.851 0.040 9 121660124 intron variant G/A snv 0.28
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2017 2017