Disease: Body mass index
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 16
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 14
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 20
rs571312 1.000 0.080 18 60172536 intergenic variant C/A snv 0.26 6
rs645040 3 136207780 upstream gene variant G/T snv 0.77 6
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 8
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 17
rs8082812 0.851 0.120 18 8522684 intergenic variant C/A snv 4.6E-02 16
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs8027181
ADPGK-AS1
15 72796528 intron variant A/T snv 0.57 2
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 36
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19