Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799929
NAT2
0.776 0.240 8 18400484 synonymous variant C/T snv 0.36 0.36 11
rs6022999
CYP24A1
0.790 0.160 20 54171474 intron variant A/G snv 0.36 9
rs12953717
SMAD7
0.724 0.240 18 48927559 intron variant C/T snv 0.36 18
rs12485716
CASR
0.925 0.080 3 122260843 intron variant G/A snv 0.36 2
rs7987649
FLT1
0.925 0.080 13 28320278 intron variant A/G snv 0.35 4
rs7656411
TLR2
0.790 0.320 4 153706503 downstream gene variant T/G snv 0.35 8
rs719725 0.827 0.080 9 6365683 intergenic variant A/C snv 0.34 7
rs230490
LOC105377621
0.882 0.080 4 102466262 downstream gene variant G/A snv 0.34 3
rs961253 0.732 0.240 20 6423634 intergenic variant C/A snv 0.34 15
rs2736118
TERT
0.882 0.120 5 1260080 intron variant T/C snv 0.33 4
rs4147542
ADH1C ; ADH1B
0.882 0.160 4 99347396 intron variant T/C snv 0.33 3
rs2853668 0.882 0.080 5 1299910 upstream gene variant G/T snv 0.33 5
rs2099902
MBL2
0.925 0.080 10 52766089 3 prime UTR variant T/C snv 0.33 2
rs8073069
BIRC5
0.807 0.200 17 78213692 upstream gene variant G/C snv 0.33 7
rs14035
RAN
0.742 0.320 12 130876696 3 prime UTR variant C/T snv 0.33 15
rs4932178
FURIN
0.925 0.080 15 90868426 upstream gene variant C/T snv 0.32 2
rs12527379 1.000 0.080 6 131958700 intron variant G/A snv 0.31 1
rs2279744
MDM2
0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs1979277
SHMT1
0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 45
rs2302615
ODC1-DT ; SNORA80B ; ODC1
0.807 0.120 2 10448012 intron variant C/T snv 0.31 7
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs10934578
CASR
0.925 0.080 3 122258435 intron variant G/T snv 0.30 4
rs2870820
MDM2
0.851 0.120 12 68808546 intron variant C/T snv 0.30 4
rs8176318
BRCA1
0.807 0.120 17 43045257 3 prime UTR variant C/A snv 0.34 0.29 6