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: rs1935
rs1935
10 63168063 missense variant C/A;G;T snv 4.0E-06; 0.44
CUI: C0242216
Disease: Biliary calculi
Biliary calculi
0.700 1.000 1 2018 2018
dbSNP: rs10822145
rs10822145
10 63174788 intron variant C/T snv 0.44
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 2 2015 2018
dbSNP: rs35997229
rs35997229
1.000 0.080 10 63197831 intron variant T/C;G snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.700 1.000 1 2017 2017
dbSNP: rs4379723
rs4379723
10 63203689 intron variant T/C snv 0.43
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.800 1.000 2 2013 2019
dbSNP: rs41274072
rs41274072
10 63214396 missense variant T/C snv 2.9E-02 5.3E-02
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs7916868
rs7916868
10 63229171 intron variant A/T snv 0.47
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.700 1.000 2 2016 2017
dbSNP: rs7916868
rs7916868
10 63229171 intron variant A/T snv 0.47
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs7916868
rs7916868
10 63229171 intron variant A/T snv 0.47
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018
dbSNP: rs7082066
rs7082066
10 63239211 intron variant A/G snv 0.69
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 1 2019 2019
dbSNP: rs7082066
rs7082066
10 63239211 intron variant A/G snv 0.69
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
0.700 1.000 1 2019 2019
dbSNP: rs7902343
rs7902343
10 63245639 intron variant C/T snv 0.40
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018
dbSNP: rs7902343
rs7902343
10 63245639 intron variant C/T snv 0.40
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs6479891
rs6479891
1.000 0.120 10 63246696 intron variant T/A;C snv
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis
0.800 1.000 1 2012 2012
dbSNP: rs9415676
rs9415676
10 63250866 intron variant A/G snv 0.44
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 1.000 1 2019 2019
dbSNP: rs10995477
rs10995477
10 63250912 intron variant T/C snv 0.43
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs10995477
rs10995477
10 63250912 intron variant T/C snv 0.43
CUI: C0857490
Disease: Granulocyte count
Granulocyte count
0.700 1.000 1 2016 2016
dbSNP: rs10995477
rs10995477
10 63250912 intron variant T/C snv 0.43
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2016 2016
dbSNP: rs10995477
rs10995477
10 63250912 intron variant T/C snv 0.43
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs4454603
rs4454603
10 63252990 intron variant C/T snv 0.43
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2018 2018
dbSNP: rs7088799
rs7088799
10 63256414 intron variant T/G snv 0.38
CUI: C2697758
Disease: Interleukin 10 Measurement
Interleukin 10 Measurement
0.700 1.000 1 2017 2017
dbSNP: rs10761731
rs10761731
10 63267850 intron variant A/T snv 0.38
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 4 2010 2019
dbSNP: rs10761731
rs10761731
10 63267850 intron variant A/T snv 0.38
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.800 1.000 3 2011 2019
dbSNP: rs10761731
rs10761731
10 63267850 intron variant A/T snv 0.38
High density lipoprotein measurement
0.700 1.000 1 2016 2016
dbSNP: rs10761731
rs10761731
10 63267850 intron variant A/T snv 0.38
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2016 2016
dbSNP: rs10761731
rs10761731
10 63267850 intron variant A/T snv 0.38
CUI: C2697760
Disease: Interleukin 12 Measurement
Interleukin 12 Measurement
0.700 1.000 1 2017 2017