Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs782414948
CUX1
1.000 0.040 7 102227624 missense variant G/A snv 3.2E-05 2.8E-05 1
rs781754593
TNFRSF1B
1.000 0.040 1 12202039 missense variant A/G snv 4.2E-06 1
rs781172058
CXCR4
0.732 0.320 2 136115340 synonymous variant C/T snv 4.0E-06 16
rs776728511
EGF
0.925 0.040 4 109945192 missense variant A/G snv 4.0E-06 2
rs77633900
ETFA
1.000 0.040 15 76246118 intron variant G/C snv 6.3E-02 2
rs773919809
MGMT
0.763 0.200 10 129766957 missense variant C/T snv 2.0E-05 13
rs7727115
MIR3142 ; MIR3142HG
1.000 0.040 5 160474732 intron variant G/T snv 0.17 1
rs770617145
LOC100288866 ; NGFR
1.000 0.040 17 49512716 missense variant G/A snv 3.4E-05 1
rs769790595
IL4R
0.827 0.120 16 27360785 missense variant G/A;C snv 2.0E-05; 4.0E-06 5
rs766914563
LOC112268426 ; CXCR4
0.732 0.320 2 136115082 synonymous variant C/T snv 7.0E-06 16
rs7667298
KDR
0.827 0.120 4 55125564 5 prime UTR variant T/C snv 0.48 7
rs762541432
BDNF-AS ; BDNF
1.000 0.040 11 27657901 missense variant T/C snv 4.0E-06 1
rs760031382
PAX5
0.851 0.040 9 36966613 missense variant C/T snv 8.0E-06 5
rs7581886
NPAS2
0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs7572263
C2orf80
1.000 0.040 2 208186862 intron variant A/G snv 0.27 2
rs753152604
CDK4
0.827 0.040 12 57751680 missense variant C/A snv 7
rs75061358 0.882 0.040 7 54848587 intergenic variant T/C;G snv 4
rs7502563
RPTOR
0.882 0.040 17 80947993 intron variant G/A snv 0.34 3
rs749124997
LINC02456 ; HELLPAR ; IGF1
1.000 0.040 12 102402539 missense variant C/T snv 4.0E-06 1
rs745934102
PDPN
0.882 0.040 1 13607281 missense variant G/A snv 3.2E-05 1.4E-05 5
rs730437
EGFR
0.925 0.120 7 55147325 intron variant A/C snv 0.51 2
rs7300686 1.000 0.040 12 128062664 intron variant C/A;T snv 1
rs727878
EFEMP1
1.000 0.040 2 55892522 intron variant C/T snv 0.40 1
rs72554204
XRCC1
0.827 0.120 19 43546062 missense variant C/T snv 1.2E-04 1.3E-04 5
rs723527
EGFR
0.882 0.040 7 55067179 intron variant A/G snv 0.53 4