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: rs9269853
rs9269853
1.000 0.080 6 32582545 intron variant A/C;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2019 2019
dbSNP: rs2454138
rs2454138
0.925 0.120 6 32602624 intergenic variant G/A snv 0.27
CUI: C0201278
Disease: Antibody measurement (procedure)
Antibody measurement (procedure)
0.700 1.000 1 2019 2019
dbSNP: rs477515
rs477515
0.790 0.400 6 32601914 intergenic variant G/A snv 0.27
CUI: C0201278
Disease: Antibody measurement (procedure)
Antibody measurement (procedure)
0.700 1.000 1 2013 2013
dbSNP: rs1064713
rs1064713
1.000 0.080 6 32578889 3 prime UTR variant G/A;C;T snv 2.6E-02 2.1E-02
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2019 2019
dbSNP: rs545366210
rs545366210
1.000 0.080 6 32586302 intron variant T/C snv
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2019 2019
dbSNP: rs7760841
rs7760841
1.000 0.080 6 32607091 intergenic variant C/T snv 0.14
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2019 2019
dbSNP: rs2647074
rs2647074
6 32606583 intergenic variant C/T snv 0.30
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement
0.700 1.000 1 2018 2018
dbSNP: rs1059362
rs1059362
6 32580773 synonymous variant G/A snv 7.2E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs113399573
rs113399573
6 32591382 upstream gene variant C/T snv 0.23
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs116763083
rs116763083
6 32602155 intergenic variant T/A snv 4.4E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs2647074
rs2647074
6 32606583 intergenic variant C/T snv 0.30
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs28366255
rs28366255
6 32591705 upstream gene variant C/A;T snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs9256938
rs9256938
6 32579417 intron variant C/A;G snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs9270637
rs9270637
6 32597873 intergenic variant A/C;G snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs9270891
rs9270891
6 32604051 intergenic variant T/G snv 0.60
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs2647062
rs2647062
6 32602640 intergenic variant A/C snv 0.13
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2018 2018
dbSNP: rs11753207
rs11753207
1.000 0.040 6 32584671 intron variant A/C snv 0.12
Child Development Disorders, Pervasive
0.700 1.000 1 2017 2017
dbSNP: rs142790902
rs142790902
1.000 0.040 6 32582137 intron variant T/C snv 6.0E-02
Child Development Disorders, Pervasive
0.700 1.000 1 2017 2017
dbSNP: rs144660248
rs144660248
1.000 0.040 6 32583926 intron variant G/T snv
Child Development Disorders, Pervasive
0.700 1.000 1 2017 2017
dbSNP: rs2760981
rs2760981
1.000 0.040 6 32597688 intergenic variant G/A;C;T snv
Child Development Disorders, Pervasive
0.700 1.000 1 2017 2017
dbSNP: rs28724212
rs28724212
1.000 0.040 6 32588824 intron variant A/G snv
Child Development Disorders, Pervasive
0.700 1.000 1 2017 2017
dbSNP: rs41293179
rs41293179
1.000 0.040 6 32582101 intron variant C/G;T snv
Child Development Disorders, Pervasive
0.700 1.000 1 2017 2017
dbSNP: rs9270074
rs9270074
1.000 0.040 6 32586352 intron variant T/C snv
Child Development Disorders, Pervasive
0.700 1.000 1 2017 2017
dbSNP: rs9270750
rs9270750
0.925 0.120 6 32600569 intergenic variant G/A snv 0.52
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
0.700 1.000 1 2016 2016
dbSNP: rs9271060
rs9271060
1.000 0.040 6 32607736 intergenic variant C/A;G snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2016 2016