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: rs12075
rs12075
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.800 1.000 2 2011 2019
dbSNP: rs12075
rs12075
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2012 2012
dbSNP: rs12075
rs12075
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012
dbSNP: rs2814778
rs2814778
0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure)
0.800 1.000 1 2011 2019
dbSNP: rs2814778
rs2814778
0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.800 1.000 1 2012 2019
dbSNP: rs2814778
rs2814778
0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25
CUI: C2698399
Disease: Myeloperoxidase Measurement
Myeloperoxidase Measurement
0.700 1.000 1 2013 2013
dbSNP: rs3027001
rs3027001
1.000 0.040 1 159199673 intron variant C/G;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs3027012
rs3027012
1 159204333 5 prime UTR variant C/T snv 0.13
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs3027012
rs3027012
1 159204333 5 prime UTR variant C/T snv 0.13
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2012 2012
dbSNP: rs3027012
rs3027012
1 159204333 5 prime UTR variant C/T snv 0.13
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012
dbSNP: rs863002
rs863002
1 159205130 intron variant C/T snv 0.28
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2011 2011
dbSNP: rs863002
rs863002
1 159205130 intron variant C/T snv 0.28
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012
dbSNP: rs863006
rs863006
1 159207958 non coding transcript exon variant G/A snv 0.56
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012