Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7242481
ELP2 ; SLC39A6
0.925 0.080 18 36129254 5 prime UTR variant G/A snv 0.35 2
rs121913082
FAS
1.000 0.040 10 89014205 missense variant A/G snv 2
rs121913083
FAS
1.000 0.040 10 89008907 missense variant A/G snv 2
rs121913084
FAS
1.000 0.040 10 89010779 missense variant T/C snv 2
rs4785204
HEATR3
1.000 0.040 16 50069823 intron variant C/T snv 8.6E-02 2
rs549467183
MSH2
0.925 0.080 2 47475228 missense variant G/A snv 1.3E-04 3.5E-05 2
rs7182283
NEIL1
0.925 0.120 15 75351418 intron variant G/T snv 0.43 2
rs1670661
NELL1
1.000 0.040 11 21209124 intron variant C/G;T snv 2
rs1047325
S100A2
1.000 0.040 1 153561551 missense variant C/T snv 7.1E-02 0.16 2
rs10759637
SLC31A1 ; CDC26
1.000 0.040 9 113262744 3 prime UTR variant A/C snv 0.47 2
rs17761864
SMG6
1.000 0.040 17 2268343 intron variant C/A snv 0.28 2
rs754626
SRC
0.925 0.080 20 37388937 intron variant T/G snv 0.25 2
rs2239612
ST6GAL1
1.000 0.040 3 187075454 intron variant G/A snv 0.17 2
rs12296850 0.925 0.080 12 100426307 downstream gene variant A/G snv 8.7E-02 3
rs7309332 1.000 0.040 12 7938243 upstream gene variant T/C snv 0.59 3
rs74664507 1.000 0.040 9 16913838 upstream gene variant T/A snv 3
rs3138035
CCL8
0.882 0.080 17 34318930 upstream gene variant C/T snv 0.27 3
rs4822983
CHEK2
0.925 0.080 22 28719078 intron variant C/T snv 0.33 3
rs144594252
DDR2
0.882 0.080 1 162754625 missense variant C/G snv 6.8E-05 5.6E-05 3
rs267598140
DDR2
0.925 0.080 1 162778600 missense variant T/A;G snv 3
rs4268748
DEF8
0.925 0.080 16 89960104 intron variant T/C snv 0.30 3
rs12934561
IL32
0.882 0.080 16 3068864 intron variant T/C snv 0.57 3
rs804270
NEIL2
0.882 0.080 8 11770112 5 prime UTR variant G/C;T snv 3
rs181696
PLCH1
0.925 0.080 3 155548315 intron variant T/C snv 0.55 3
rs2847281
PTPN2
1.000 0.040 18 12821594 intron variant A/G snv 0.32 3