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: rs273505
rs273505
19 18106337 intron variant T/C snv 0.48
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs10401175
rs10401175
19 18119464 intron variant C/A;G snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs2072490
rs2072490
19 18146940 synonymous variant C/G;T snv 0.53
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs273504
rs273504
19 18104437 intron variant A/G snv 0.46
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs273510
rs273510
19 18112540 intron variant A/G snv 0.33
CUI: C0523677
Disease: Glycine measurement
Glycine measurement
0.700 1.000 1 2019 2019
dbSNP: rs56338130
rs56338130
19 18125061 intron variant C/T snv 0.22
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 1.000 1 2019 2019
dbSNP: rs60146811
rs60146811
19 18110403 intron variant G/A snv 0.24
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019
dbSNP: rs60146811
rs60146811
19 18110403 intron variant G/A snv 0.24
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs273506
rs273506
19 18110837 intron variant C/A;T snv
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
Digestive System Diseases 0.010 1.000 1 2008 2008
dbSNP: rs8108738
rs8108738
19 18144549 missense variant G/A snv 0.53 0.47
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
Digestive System Diseases 0.010 1.000 1 2008 2008