Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11160119
rs11160119
14 93465912 intron variant G/A snv 0.38
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs12147136
rs12147136
14 93605958 intron variant A/C snv 0.69
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2018 2018
dbSNP: rs1242889
rs1242889
14 93584824 intron variant C/A;G snv
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs2273640
rs2273640
14 93332875 synonymous variant G/A snv 0.22 0.16
CUI: C0337443
Disease: Sodium measurement
Sodium measurement
0.700 1.000 1 2018 2018
dbSNP: rs55882426
rs55882426
14 93654366 intron variant C/T snv 0.41
body fat percentage (physical finding)
0.700 1.000 1 2019 2019
dbSNP: rs6575340
rs6575340
14 93557626 intron variant G/A snv 0.61
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs6575340
rs6575340
14 93557626 intron variant G/A snv 0.61
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs7151505
rs7151505
14 93534596 intron variant G/A;C snv
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs729050
rs729050
14 93643156 intron variant G/T snv 0.75
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2017 2017
dbSNP: rs79866114
rs79866114
14 93497217 missense variant C/G snv 1.4E-02 1.3E-02
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs8007087
rs8007087
14 93452539 intron variant C/G;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs942066
rs942066
14 93565568 intron variant A/G snv 0.61
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs9989178
rs9989178
14 93541734 intron variant G/A snv 0.59
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019