Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 16
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 14
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 9
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 7
rs10198175 0.925 0.080 2 20934123 intergenic variant A/G snv 0.93 3
rs1950038 0.925 0.080 2 183579642 regulatory region variant T/C snv 0.71 2
rs73057489 0.925 0.080 12 17370820 regulatory region variant A/C snv 3.9E-02 2
rs7337127 0.925 0.080 13 104623579 intergenic variant C/A;T snv 2
rs6006893
ARHGAP8 ; PRR5-ARHGAP8
0.925 0.080 22 44858015 intron variant C/T snv 0.15 2
rs726170
ARHGAP8 ; PRR5-ARHGAP8
0.925 0.080 22 44855931 intron variant C/T snv 0.15 2
rs17810023
BCKDHB
0.925 0.080 6 80443056 non coding transcript exon variant C/T snv 1.7E-02 2
rs7904579
CUBN
0.925 0.080 10 17089754 intron variant G/A;C snv 2
rs111940429
LINC01789
0.925 0.080 2 107366232 intron variant C/A;T snv 2
rs76087671
LOC105372577
0.925 0.080 20 24330541 intergenic variant C/A;G;T snv 2
rs182107583
MMADHC-DT
0.925 0.080 2 149675023 intron variant A/C snv 4.2E-03 2
rs145763646
SLC25A26
0.925 0.080 3 66173478 intron variant G/A snv 0.13 2
rs372794914
MC4R
0.925 0.080 18 60372319 missense variant T/C snv 6.0E-05 2.8E-05 1