Source: GWASCAT

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: rs4734879
rs4734879
8 105570896 intron variant A/G snv 0.31
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 1.000 1 2019 2019
dbSNP: rs4734879
rs4734879
8 105570896 intron variant A/G snv 0.31
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs57942103
rs57942103
1.000 0.040 8 105501233 intron variant A/C snv 0.25
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs57942103
rs57942103
1.000 0.040 8 105501233 intron variant A/C snv 0.25
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.700 1.000 1 2019 2019
dbSNP: rs57942103
rs57942103
1.000 0.040 8 105501233 intron variant A/C snv 0.25
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE
0.700 1.000 1 2019 2019
dbSNP: rs6993770
rs6993770
0.925 0.080 8 105569300 intron variant A/T snv 0.31
CUI: C2697760
Disease: Interleukin 12 Measurement
Interleukin 12 Measurement
0.700 1.000 1 2017 2017
dbSNP: rs6993770
rs6993770
0.925 0.080 8 105569300 intron variant A/T snv 0.31
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs6993770
rs6993770
0.925 0.080 8 105569300 intron variant A/T snv 0.31
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs6993770
rs6993770
0.925 0.080 8 105569300 intron variant A/T snv 0.31
Platelet Component Distribution Width Measurement
0.700 1.000 1 2016 2016
dbSNP: rs6993770
rs6993770
0.925 0.080 8 105569300 intron variant A/T snv 0.31
Platelet mean volume determination (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs72679151
rs72679151
8 104614889 intron variant C/T snv 0.17
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs7819593
rs7819593
8 105102944 intron variant T/C snv 0.35
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2019 2019
dbSNP: rs7832219
rs7832219
8 105566749 intron variant T/C snv 0.31
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs7837523
rs7837523
8 105517074 intron variant A/T snv 0.80
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs9297357
rs9297357
0.851 0.040 8 105130105 intron variant C/G;T snv
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 1.000 1 2013 2013
dbSNP: rs9297357
rs9297357
0.851 0.040 8 105130105 intron variant C/G;T snv
Child Development Disorders, Pervasive
0.700 1.000 1 2013 2013
dbSNP: rs9297357
rs9297357
0.851 0.040 8 105130105 intron variant C/G;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 1.000 1 2013 2013
dbSNP: rs9297357
rs9297357
0.851 0.040 8 105130105 intron variant C/G;T snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.700 1.000 1 2013 2013