Disease: Body mass index procedure
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13013484 2 27765954 intergenic variant G/A snv 0.61 3
rs13034723
C2orf88
2 190120954 intron variant G/A snv 0.37 2
rs1320336 2 650012 intergenic variant G/A snv 0.18 2
rs1320337 2 649867 intergenic variant A/T snv 0.19 2
rs1320338 2 649347 intergenic variant T/G snv 0.18 2
rs13386517 2 650479 regulatory region variant G/A;C snv 2
rs13386627 2 650560 regulatory region variant G/C;T snv 2
rs13386964 2 650828 regulatory region variant G/A snv 0.18 2
rs13388043 2 637597 regulatory region variant C/A;T snv 2
rs13393304 2 637830 regulatory region variant A/C;G snv 2
rs13396935 2 653195 intergenic variant G/A snv 0.18 2
rs13397165 2 653354 intergenic variant G/A snv 0.18 2
rs13401686 2 650519 regulatory region variant A/G snv 0.18 2
rs13415094 2 653093 intergenic variant T/C snv 0.19 2
rs149954327
STON1-GTF2A1L ; STON1
2 48582005 missense variant T/G snv 6.8E-05 1.2E-04 2
rs1561288
EFR3B
2 25146133 3 prime UTR variant C/T snv 0.29 2
rs2068834
ZNF512
0.925 0.120 2 27616672 intron variant T/C snv 0.28 10
rs2867108 2 650143 intergenic variant T/C snv 0.18 2
rs2867109 2 651030 regulatory region variant T/G snv 0.18 2
rs2867110 2 651105 regulatory region variant G/C snv 0.18 2
rs2867112 2 651349 intergenic variant T/G snv 0.18 2
rs2867113 2 651365 intergenic variant G/A snv 0.18 2
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 3
rs2890652 2 142202362 intergenic variant T/C snv 0.21 2
rs2903492 2 624678 intergenic variant G/A snv 0.85 2