Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1005230
VEGFA
0.827 0.040 6 43768759 upstream gene variant T/C snv 0.60 5
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs10116277
CDKN2B-AS1
0.827 0.160 9 22081398 intron variant G/T snv 0.62 8
rs10120688
CDKN2B-AS1
0.807 0.080 9 22056500 intron variant G/A snv 0.50 7
rs10131
LIG4
1.000 0.040 13 108207498 3 prime UTR variant C/T snv 0.12 3
rs10131032
AKAP6
1.000 0.040 14 32780875 intron variant G/A snv 9.3E-02 2
rs10165970
NPAS2
0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs1034749666
OLIG2
0.776 0.160 21 33027257 missense variant G/A snv 9
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1044129
AVEN ; RYR3
0.790 0.200 15 33866065 3 prime UTR variant A/G;T snv 9
rs1045485
CASP8
0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs10464870
CCDC26
0.882 0.040 8 129465577 intron variant C/T snv 0.80 3
rs1048771
RAD54L ; LRRC41
1.000 0.040 1 46278228 synonymous variant C/A;T snv 4.0E-06; 0.15 1
rs104894104
CDKN2A
0.790 0.160 9 21971019 missense variant G/A;T snv 7
rs104894156
DMBT1
1.000 0.040 10 122582793 missense variant G/T snv 1
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs10494090
SLC25A24
1.000 0.040 1 108150714 intron variant A/C;G;T snv 2
rs10506868
VTI1A
0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 16
rs10519097
RORA
0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs1052555
ERCC2
0.882 0.040 19 45352266 synonymous variant G/A snv 0.28 0.26 3
rs1052576
CASP9
0.807 0.200 1 15506048 missense variant T/A;C snv 0.53 9
rs1053667
TOGARAM1
0.925 0.120 14 45073835 3 prime UTR variant T/C snv 0.11 4
rs1057519902
H3-3A
0.742 0.160 1 226064451 missense variant G/C snv 16
rs1057519903
H3-3A
0.683 0.080 1 226064434 missense variant A/T snv 28