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: rs1808579
rs1808579
18 23524924 intron variant C/T snv 0.47
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 4 2015 2019
dbSNP: rs1788820
rs1788820
18 23521980 intron variant A/G snv 0.69
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2017 2018
dbSNP: rs177430
rs177430
18 23506161 intron variant C/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2017 2017
dbSNP: rs1788799
rs1788799
1.000 0.080 18 23544981 missense variant C/A;G;T snv 4.2E-06; 0.73
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2018 2018
dbSNP: rs1788808
rs1788808
18 23510059 intron variant A/C;G snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs6507716
rs6507716
18 23535096 intron variant A/G snv 0.51
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2015 2015
dbSNP: rs891387
rs891387
18 23523945 intron variant T/C snv 0.55
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019