Disease: Body mass index
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10408163
ZC3H4
19 47093845 non coding transcript exon variant T/C snv 0.52 6
rs12328675
COBLL1
2 164684290 3 prime UTR variant T/C snv 0.13 4
rs306890
SPRY3
Y 56944005 intergenic variant T/C snv 4
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs645040 3 136207780 upstream gene variant G/T snv 0.77 6
rs7200543
PDXDC1
16 15036113 synonymous variant A/G snv 0.35 0.30 6
rs730180
BBS4
15 72715552 intron variant G/A snv 0.72 2
rs75766425
NID2
14 52045193 intron variant G/C snv 3.0E-03 2
rs8027181
ADPGK-AS1
15 72796528 intron variant A/T snv 0.57 2
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 21
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 43
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 25
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 36
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 38
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 23
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 23
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 19
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 11
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 20
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19