Disease: Body mass index
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs12328675
COBLL1
2 164684290 3 prime UTR variant T/C snv 0.13 4
rs306890
SPRY3
Y 56944005 intergenic variant T/C snv 4
rs2304130
ZNF101
1.000 0.080 19 19678719 splice region variant A/G snv 0.10 0.12 5
rs10408163
ZC3H4
19 47093845 non coding transcript exon variant T/C snv 0.52 6
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
rs7200543
PDXDC1
16 15036113 synonymous variant A/G snv 0.35 0.30 6
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 7
rs7607980
COBLL1
1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 7
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv 7
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 8
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 11
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 11
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 14
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12369179
ZCCHC8
0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 16