Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs2291599
DKK3
0.925 0.120 11 11968352 intron variant T/C snv 0.83 0.85 2
rs7396187
DKK3
0.925 0.120 11 11967604 intron variant C/G snv 0.84 2
rs132770
DESI1 ; XRCC6
0.752 0.320 22 41621260 5 prime UTR variant A/G snv 0.83 14
rs8081059
SLC39A11
0.925 0.120 17 73072580 intron variant C/A snv 0.83 2
rs3206824
DKK3
0.827 0.160 11 11964514 missense variant T/C snv 0.78 0.78 6
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs3118523 0.925 0.120 9 134443675 downstream gene variant G/A snv 0.75 2
rs333951
CSF1
0.925 0.120 1 109909068 upstream gene variant T/C snv 0.74 2
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs6466135 0.925 0.120 7 106861053 upstream gene variant A/G snv 0.71 2
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1609682
IL1A
0.882 0.160 2 112782628 intron variant G/T snv 0.70 3
rs3783546
IL1A
0.882 0.160 2 112777253 intron variant G/C snv 0.70 5
rs3783550
IL1A
0.827 0.200 2 112775308 intron variant G/T snv 0.64 0.70 5
rs1049380
ITPR2
0.827 0.120 12 26336611 3 prime UTR variant G/T snv 0.69 5
rs1805105
AXIN1
0.776 0.280 16 346264 synonymous variant A/G snv 0.61 0.69 11
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs132774
XRCC6
0.776 0.280 22 41635949 intron variant C/G snv 0.69 9
rs5751129
XRCC6 ; DESI1
0.752 0.320 22 41619761 intron variant C/T snv 0.69 14
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1332018
GSTM5 ; GSTM3
0.882 0.200 1 109740350 5 prime UTR variant G/T snv 0.64 0.66 6
rs8101626
DNMT1
1.000 0.120 19 10135353 intron variant G/A snv 0.64 1
rs7132434 0.925 0.120 12 26319629 non coding transcript exon variant A/G snv 0.62 2
rs448012
FLT4
0.925 0.120 5 180619344 missense variant G/C snv 0.63 0.61 2