Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs494558
COL4A1
13 110276815 intron variant C/T snv 0.90 2
rs7187961
FTO
16 53792122 intron variant T/C snv 0.86 2
rs7261964
PIGU
20 34617207 intron variant C/T snv 0.85 1
rs6793368
LOC105374257 ; DGKG
3 186122654 intron variant C/T snv 0.82 1
rs7561317 0.925 0.120 2 644953 intergenic variant A/G snv 0.81 7
rs7948458
IGF2 ; INS-IGF2
11 2151600 intron variant A/C snv 0.76 1
rs9374842 6 119864519 regulatory region variant C/T snv 0.76 2
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 8
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 9
rs12705992 7 114789947 regulatory region variant G/A snv 0.72 1
rs6416056
BDNF-AS ; LINC00678
11 27625198 intron variant G/A snv 0.71 1
rs29941 1.000 0.080 19 33818627 downstream gene variant A/G snv 0.70 6
rs2256174
MICA
6 31412645 intron variant A/G snv 0.64 1
rs6499640
FTO
0.925 0.160 16 53735765 intron variant G/A snv 0.59 7
rs10198628 2 12824371 intron variant A/G snv 0.59 2
rs4145878
H3C4 ; H2BC7
6 26197818 intron variant T/A snv 0.58 1
rs7624084
ZBTB38
3 141374443 intron variant T/C snv 0.54 3
rs965178 18 25681256 intergenic variant T/C snv 0.53 1
rs1973993 1 96478438 intergenic variant T/C snv 0.49 1
rs6440919 3 153982187 upstream gene variant C/T snv 0.47 1
rs2531995
ADCY9
1.000 0.080 16 3963466 3 prime UTR variant C/T snv 0.45 7
rs143384
GDF5
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 17
rs765876
HIVEP2
6 142864754 intron variant A/G snv 0.43 1
rs6864091
POC5
5 75714177 intron variant T/C snv 0.43 2
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32