Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1724120
ASTL ; DUSP2
0.925 0.080 2 96143592 3 prime UTR variant T/C snv 0.53 2
rs1342387
ADIPOR1
0.776 0.120 1 202945228 intron variant T/C snv 0.53 12
rs4803455
TGFB1
0.752 0.280 19 41345604 intron variant C/A snv 0.51 11
rs2189517
RAD51B
0.882 0.080 14 68536271 intron variant A/G snv 0.49 3
rs2854744
IGFBP3
0.695 0.520 7 45921476 intron variant G/T snv 0.48 20
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs3804099
TLR2
0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs712
KRAS
0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs12490683
LOC105377207 ; MYLKP1
0.925 0.080 3 75329934 non coding transcript exon variant G/A snv 0.46 2
rs2585428
CYP24A1
0.763 0.200 20 54170358 intron variant C/T snv 0.46 11
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs10222633
CASR
0.925 0.080 3 122258079 intron variant G/A snv 0.45 4
rs4696480
TLR2
0.716 0.400 4 153685974 intron variant T/A snv 0.45 19
rs13281615
CASC8 ; POU5F1B ; PCAT1 ; CASC21
0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 23
rs12591359
MIR4713HG ; CYP19A1
0.925 0.080 15 51247171 intron variant G/A snv 0.41 4
rs374400
OBSCN
0.925 0.080 1 228347383 intron variant C/T snv 0.40 2
rs2304204
BCL2L12 ; IRF3
0.882 0.160 19 49665763 5 prime UTR variant T/C snv 0.39 3
rs9344
CCND1
0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 34
rs2236225
MTHFD1
0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs2555639 0.851 0.080 4 174540379 non coding transcript exon variant T/C snv 0.38 7
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs187115
CD44
0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs2167270
LEP
0.724 0.280 7 128241296 5 prime UTR variant G/A snv 0.37 17
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62