Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10090787
LOC107986874 ; SNTB1
1.000 0.080 8 120798309 intron variant C/T snv 0.34 3
rs1816158
MIR100HG
0.925 0.200 11 122155752 intron variant C/A;T snv 3
rs34329
CDKN1B
1.000 0.080 12 12720299 intron variant G/C snv 0.61 2
rs7778413
SND1
1.000 0.080 7 127717662 intron variant T/C snv 0.23 2
rs3757769
SND1
1.000 0.080 7 127901009 intron variant A/G snv 9.7E-02 2
rs7799039
LOC105375494
0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs987525
CCDC26
0.807 0.160 8 128933908 intron variant C/A snv 0.31 7
rs12917
MGMT ; LOC105378560
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs928674
LAMC3
0.827 0.080 9 131076637 intron variant A/G snv 0.16 6
rs77452476
LAMC3
0.827 0.080 9 131087186 intron variant T/G snv 0.18 7
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs3813867
LOC107984284 ; CYP2E1
0.732 0.240 10 133526101 intron variant G/A;C snv 13
rs2031920
LOC107984284 ; CYP2E1
0.695 0.240 10 133526341 non coding transcript exon variant C/T snv 3.1E-02 20
rs10462706
CLPTM1L
0.827 0.080 5 1343679 intron variant C/T snv 0.14 6
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2040639
XRCC2
1.000 0.080 7 152678103 upstream gene variant T/C;G snv 2
rs4696480
TLR2
0.716 0.400 4 153685974 intron variant T/A snv 0.45 19
rs2120243
VEPH1
0.925 0.200 3 157429779 intron variant A/C snv 0.59 3
rs3816527
PTX3 ; VEPH1
0.882 0.160 3 157437525 missense variant C/A snv 0.64 0.64 9
rs221236 1.000 0.120 7 157529938 downstream gene variant G/A snv 0.96 2
rs3212227
IL12B
0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs629849
IGF2R
0.827 0.160 6 160073377 missense variant A/C;G;T snv 0.90 0.91 9
rs2046463
LOC105377555
1.000 0.080 4 176681548 intron variant G/A;C snv 3
rs7664413
VEGFC ; LOC105377555
0.851 0.160 4 176687553 intron variant C/T snv 0.24 0.25 7