Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6489769
RAD52
0.851 0.120 12 963799 intron variant C/A;T snv 4
rs485842
MAML2
1.000 0.040 11 96290050 intron variant C/T snv 0.26 1
rs4598633
MAML2
1.000 0.040 11 96278187 intron variant T/A;C snv 1
rs7115578
MAML2
0.882 0.040 11 96266936 intron variant G/A snv 0.37 3
rs7938889
MAML2
1.000 0.040 11 96231355 intron variant C/T snv 0.48 1
rs7107785
MAML2
1.000 0.040 11 96014174 intron variant T/C snv 0.57 2
rs3751667
LMF1
1.000 0.040 16 954554 synonymous variant C/T snv 0.28 0.29 4
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
rs11571378
RAD52
0.925 0.080 12 950115 intron variant A/C;T snv 2
rs7963551
RAD52
0.807 0.160 12 912349 3 prime UTR variant T/G snv 0.13 7
rs118101777
IDH2
0.614 0.280 15 90087472 missense variant C/T snv 2.0E-03 1.6E-03 42
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs786204929
PTEN
0.752 0.200 10 87933144 stop gained G/A;T snv 12
rs786202398
PTEN
0.925 0.080 10 87925518 stop gained T/A;G snv 2
rs1554893792
PTEN
1.000 0.040 10 87894052 missense variant G/A snv 1
rs1064794096
KLLN ; PTEN
1.000 0.040 10 87864514 missense variant A/C;T snv 2
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1805377
XRCC4
0.689 0.480 5 83353124 splice acceptor variant G/A snv 0.23 0.25 19
rs11163687
LOC107985037
1.000 0.040 1 83199436 intergenic variant A/G snv 9.6E-02 2
rs2075685
TMEM167A ; XRCC4
0.724 0.320 5 83076846 intron variant G/A;T snv 14
rs11233250
MIR4300HG
0.882 0.040 11 82685972 intron variant C/T snv 0.11 4
rs2289591
PER1 ; MIR6883
0.882 0.080 17 8144692 stop gained C/A;G;T snv 0.17; 7.2E-06; 7.2E-06 3
rs7502563
RPTOR
0.882 0.040 17 80947993 intron variant G/A snv 0.34 3