Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2868371
HSPB1
0.827 0.120 7 76301442 upstream gene variant C/G snv 0.22 6
rs107822
MIR219A1 ; RING1
0.827 0.120 6 33207798 upstream gene variant C/T snv 0.27 0.28 5
rs4645878
BAX
0.882 0.120 19 48954681 upstream gene variant A/G snv 0.89 5
rs7631358
TP63
0.851 0.080 3 189630622 upstream gene variant G/A snv 0.13 4
rs10898880
LOC107984421 ; ATG16L2
0.925 0.160 11 72814066 upstream gene variant C/A snv 0.50 3
rs12769316
NFKB2
0.925 0.160 10 102392994 upstream gene variant G/A snv 0.13 3
rs1711972
FOXF2 ; LOC105374880
0.925 0.160 6 1388953 upstream gene variant A/C snv 4.7E-02 3
rs3138035
CCL8
0.882 0.080 17 34318930 upstream gene variant C/T snv 0.27 3
rs421446
MIR219A1 ; RING1 ; HSD17B8
0.882 0.280 6 33207006 upstream gene variant A/G snv 0.32 3
rs10503380 1.000 0.080 8 9552985 upstream gene variant C/T snv 0.25 2
rs11622887
SYNE3
1.000 0.080 14 95476110 upstream gene variant A/C snv 0.52 2
rs4929984
MRPL23 ; H19
0.925 0.160 11 2003453 upstream gene variant C/A snv 2
rs11674251 1.000 0.080 2 20016748 upstream gene variant T/C snv 0.18 1
rs1209950 1.000 0.080 21 38801604 upstream gene variant C/T snv 0.30 1
rs1414493 1.000 0.080 1 241523216 upstream gene variant A/G snv 0.62 1
rs1957860 1.000 0.080 14 53962637 upstream gene variant C/T snv 0.51 1
rs2227484
LOC105369818 ; IL22
1.000 0.080 12 68254149 upstream gene variant G/A snv 0.15 1
rs298206
LINC01414
1.000 0.080 8 64369942 upstream gene variant T/A;C snv 1
rs3764383
BIRC5
1.000 0.080 17 78212770 upstream gene variant C/G;T snv 1
rs652625
TNFRSF1B ; MIR7846
1.000 0.080 1 12165294 upstream gene variant T/A snv 0.14 1
rs7525160
CR1
1.000 0.080 1 207495069 upstream gene variant G/C snv 0.29 1
rs784621
HEYL
1.000 0.080 1 39641113 upstream gene variant T/C snv 0.85 1
rs937282
MDM2
1.000 0.080 12 68808017 upstream gene variant C/G snv 0.56 1
rs9660710 1.000 0.080 1 1163962 upstream gene variant A/C;T snv 1
rs397517106
EGFR-AS1 ; EGFR
1.000 0.080 7 55181287 coding sequence variant -/TCCAGGAAGCCT delins 1