Source: ALL
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: rs11842874
rs11842874
1.000 0.040 13 113040195 intron variant A/G snv 0.12
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis
Musculoskeletal Diseases 0.810 1.000 2 2011 2015
dbSNP: rs9549328
rs9549328
13 112981842 intron variant C/T snv 0.21
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 3 2017 2019
dbSNP: rs1046205
rs1046205
13 113097743 3 prime UTR variant A/T snv 0.22
CUI: C2825856
Disease: Factor VII measurement
Factor VII measurement
0.700 1.000 1 2019 2019
dbSNP: rs10665
rs10665
13 113098517 3 prime UTR variant A/G snv 0.12
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
0.700 1.000 1 2013 2013
dbSNP: rs10665
rs10665
13 113098517 3 prime UTR variant A/G snv 0.12
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs117989138
rs117989138
13 113043357 non coding transcript exon variant G/A snv 1.0E-02
CUI: C2825856
Disease: Factor VII measurement
Factor VII measurement
0.700 1.000 1 2019 2019
dbSNP: rs12019546
rs12019546
1.000 0.040 13 113005392 intron variant G/A snv 0.25
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs1317507
rs1317507
1.000 0.040 13 112977466 intron variant A/C;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs2146751
rs2146751
13 113095331 non coding transcript exon variant A/G snv 0.63
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs2146752
rs2146752
13 113095161 3 prime UTR variant G/A;C snv 0.66
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs2181540
rs2181540
13 113098850 3 prime UTR variant T/C snv 0.15
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs2181540
rs2181540
13 113098850 3 prime UTR variant T/C snv 0.15
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
0.700 1.000 1 2013 2013
dbSNP: rs2476325
rs2476325
13 113082763 intron variant A/G snv 0.79
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs2480952
rs2480952
13 113098925 3 prime UTR variant T/C snv 0.23
CUI: C2825856
Disease: Factor VII measurement
Factor VII measurement
0.700 1.000 1 2019 2019
dbSNP: rs2873281
rs2873281
13 113086288 intron variant G/A snv 0.14 0.16
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs3011549
rs3011549
13 112980623 intron variant A/C;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2017 2017
dbSNP: rs36086577
rs36086577
13 113074184 intron variant C/A snv 0.11
CUI: C2825856
Disease: Factor VII measurement
Factor VII measurement
0.700 1.000 1 2019 2019
dbSNP: rs521720
rs521720
13 113082830 intron variant C/G;T snv
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs534298
rs534298
13 113089454 intron variant T/C;G snv
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs553702
rs553702
13 113090355 intron variant A/G snv 0.83
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs71446935
rs71446935
13 113080062 intron variant A/G snv
CUI: C2825856
Disease: Factor VII measurement
Factor VII measurement
0.700 1.000 1 2019 2019
dbSNP: rs7327099
rs7327099
13 113094376 non coding transcript exon variant C/T snv 0.75
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs9324220
rs9324220
13 113088281 intron variant C/T snv 0.14 0.16
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2013 2013
dbSNP: rs9549328
rs9549328
13 112981842 intron variant C/T snv 0.21
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs766316400
rs766316400
1.000 0.040 13 113087292 missense variant G/A snv 1.4E-05
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 1.000 1 2017 2017