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: rs1588265
rs1588265
1.000 0.080 5 60073967 intron variant A/G;T snv
CUI: C0004096
Disease: Asthma
Asthma
0.800 1.000 3 2009 2011
dbSNP: rs17444059
rs17444059
5 59264891 intron variant T/C snv 8.5E-02
CUI: C2699541
Disease: Cytokine Measurement
Cytokine Measurement
0.800 1.000 1 2012 2012
dbSNP: rs1544791
rs1544791
1.000 0.080 5 60143255 intron variant T/A;C snv
CUI: C0004096
Disease: Asthma
Asthma
0.710 1.000 1 2009 2016
dbSNP: rs2548659
rs2548659
1.000 0.080 5 60088059 intron variant A/G snv 0.28
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 2 2009 2010
dbSNP: rs983280
rs983280
1.000 0.080 5 60149310 intron variant C/T snv 0.68
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 2 2009 2010
dbSNP: rs10052657
rs10052657
0.807 0.120 5 59111944 intron variant C/A snv 0.17
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus
0.700 1.000 1 2011 2011
dbSNP: rs12515974
rs12515974
5 60273696 intron variant C/T snv 0.76
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs1353747
rs1353747
0.882 0.080 5 59041654 intron variant T/G snv 6.9E-02
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.700 1.000 1 2013 2013
dbSNP: rs1823068
rs1823068
5 59380223 intron variant A/G snv 0.15
CUI: C2830004
Disease: Somnolence
Somnolence
0.700 1.000 1 2007 2007
dbSNP: rs26704
rs26704
5 59237827 intron variant A/G;T snv
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.700 1.000 1 2012 2012
dbSNP: rs6865647
rs6865647
5 59103374 intron variant A/G;T snv
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases
0.700 1.000 1 2011 2011
dbSNP: rs7732249
rs7732249
1.000 0.040 5 60070442 intron variant C/T snv 0.92
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 1.000 1 2011 2011