Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1413299
COL15A1
0.925 0.120 9 98998959 intron variant G/A;T snv 2
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs76032516
MAML2
0.925 0.120 11 96097550 intron variant A/C;T snv 2
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs17702471
GPC6
0.925 0.120 13 93224864 upstream gene variant A/G snv 0.16 2
rs4987208
RAD52
0.851 0.160 12 913403 stop gained A/C snv 3.5E-02 2.1E-02 4
rs1596797
MUC16
0.925 0.120 19 8977341 missense variant T/A;C;G snv 2.0E-05; 4.0E-06; 0.74 2
rs17130142
PKN2-AS1
1.000 0.120 1 87773925 intron variant G/A snv 6.5E-02 1
rs533117495
ABCB1
0.827 0.200 7 87595783 missense variant C/T snv 8.0E-06 5
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 9
rs9787692 1.000 0.120 10 8603200 intergenic variant T/G snv 0.30 1
rs1649942
NRG3
0.925 0.120 10 82191935 intron variant G/A;C snv 3
rs11782652
CHMP4C
0.851 0.120 8 81741409 intron variant A/G snv 6.6E-02 4
rs7643459
LOC101927394 ; LMCD1-AS1
0.925 0.120 3 7963141 intron variant G/C;T snv 2
rs192876988
LOC105377300
0.851 0.120 4 79376097 intergenic variant T/C snv 1.6E-02 4
rs3745546
INSR
0.925 0.120 19 7211805 intron variant G/A;C snv 2
rs2252673
INSR
0.882 0.120 19 7150407 intron variant C/G snv 0.75 3
rs3087714
SULF1
0.925 0.120 8 69660769 3 prime UTR variant G/A snv 0.30 2
rs10017134
UGT2A2 ; UGT2A1
0.925 0.120 4 69591303 intron variant T/C snv 0.75 2
rs4286604 0.925 0.120 4 69576447 intron variant A/G snv 0.76 2
rs17106154
RAD51B
0.925 0.120 14 68694457 non coding transcript exon variant T/C snv 7.8E-02 2