Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2232365
FOXP3
0.716 0.480 X 49259429 intron variant T/C snv 16
rs3117582
BAG6 ; APOM
0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 14
rs1800012
COL1A1
0.763 0.320 17 50200388 intron variant C/A snv 0.14 13
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv 11
rs2082940
ADIPOQ-AS1 ; ADIPOQ
0.763 0.480 3 186856375 3 prime UTR variant T/A;C snv 10
rs1194611372
S100A11
0.763 0.320 1 152032679 missense variant A/C snv 9
rs121913474
FGFR2
0.790 0.200 10 121515260 missense variant A/G snv 9
rs1456315
PRNCR1 ; PCAT1 ; CASC19
0.790 0.200 8 127091692 non coding transcript exon variant T/A;C snv 9
rs12149832
FTO
0.851 0.120 16 53808996 intron variant G/A snv 0.31 8
rs16901946
PCAT1 ; CASC19 ; PRNCR1
0.827 0.160 8 127088680 non coding transcript exon variant A/G snv 1.7E-02 8
rs5030772
FASLG
0.790 0.320 1 172664210 intron variant A/G snv 9.9E-02 7
rs7775228 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 7
rs650108
MMP3
0.827 0.160 11 102838056 intron variant G/A snv 0.31 6
rs8044769
FTO
0.851 0.200 16 53805223 intron variant T/A;C;G snv 6
rs1034528
MTOR ; ANGPTL7
0.882 0.120 1 11189075 intron variant G/C snv 0.30 5
rs121918505
FGFR2
0.851 0.080 10 121520119 missense variant A/G snv 5
rs12885713
CALM1
0.827 0.200 14 90397013 intron variant C/A;G;T snv 5
rs2929970
CCN4
0.827 0.200 8 133228894 3 prime UTR variant G/A snv 0.52 5
rs7135617
ORAI1
0.827 0.240 12 121631099 intron variant T/C;G snv 5
rs12982744
DOT1L
0.925 0.040 19 2177194 intron variant C/A;G;T snv 4
rs17039192
EPAS1
0.851 0.120 2 46297441 5 prime UTR variant C/T snv 1.9E-02 4
rs2057768 0.925 0.120 16 27310774 upstream gene variant C/A;G;T snv 4
rs2820436
LYPLAL1-AS1
0.882 0.040 1 219467338 intergenic variant A/C;G snv 4
rs10492367 0.882 0.040 12 27862037 regulatory region variant G/T snv 0.12 3
rs10947262
TSBP1-AS1 ; BTNL2
0.925 0.040 6 32405535 non coding transcript exon variant C/T snv 0.12 3