Source: GWASDB

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: rs612169
rs612169
ABO
9 133268030 intron variant G/A snv
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.800 1.000 1 2013 2017
dbSNP: rs612169
rs612169
ABO
9 133268030 intron variant G/A snv
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 1.000 2 2011 2012
dbSNP: rs612169
rs612169
ABO
9 133268030 intron variant G/A snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs612169
rs612169
ABO
9 133268030 intron variant G/A snv
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level
0.700 1.000 1 2011 2011
dbSNP: rs612169
rs612169
ABO
9 133268030 intron variant G/A snv
CUI: C0337438
Disease: Glucose measurement
Glucose measurement
0.700 1.000 1 2011 2011
dbSNP: rs612169
rs612169
ABO
9 133268030 intron variant G/A snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs612169
rs612169
ABO
9 133268030 intron variant G/A snv
CUI: C0202202
Disease: Protein measurement
Protein measurement
0.700 1.000 1 2012 2012
dbSNP: rs612169
rs612169
ABO
9 133268030 intron variant G/A snv
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2012 2012
dbSNP: rs612169
rs612169
ABO
9 133268030 intron variant G/A snv
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis
0.700 1.000 1 2012 2012
dbSNP: rs612169
rs612169
ABO
9 133268030 intron variant G/A snv
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement
0.700 1.000 1 2011 2011