Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12210050
LOC105374875
0.807 0.040 6 475489 non coding transcript exon variant C/T snv 0.11 8
rs7335046 0.807 0.040 13 99389484 downstream gene variant G/C snv 0.80 7
rs1246946 0.851 0.040 6 4979722 downstream gene variant C/T snv 0.34 4
rs4761496 0.851 0.040 12 94733833 regulatory region variant T/A;C snv 0.23 4
rs7297245
HAL
0.882 0.040 12 95980836 missense variant C/T snv 0.85 0.86 4
rs75790006 0.851 0.040 4 43211547 intron variant T/G snv 1.1E-02 4
rs2847281
PTPN2
1.000 0.040 18 12821594 intron variant A/G snv 0.32 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
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
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
rs1670661
NELL1
1.000 0.040 11 21209124 intron variant C/G;T snv 2
rs17761864
SMG6
1.000 0.040 17 2268343 intron variant C/A snv 0.28 2
rs2239612
ST6GAL1
1.000 0.040 3 187075454 intron variant G/A snv 0.17 2
rs4785204
HEATR3
1.000 0.040 16 50069823 intron variant C/T snv 8.6E-02 2
rs6413464
CDKN2A
1.000 0.040 9 21970980 missense variant C/A;G snv 1.3E-03; 4.1E-06 2
rs6503659 1.000 0.040 17 41741012 intergenic variant A/C;G;T snv 2
rs1064793400
MLH1
1.000 0.040 3 37048550 missense variant G/A snv 1
rs1064793981
MSH2
1.000 0.040 2 47475030 missense variant G/A snv 1
rs1078305
GSN
1.000 0.040 9 121289122 intron variant A/G snv 0.70 1
rs10818524
GSN
1.000 0.040 9 121267901 intron variant T/C snv 0.37 1
rs10971638
PTENP1
1.000 0.040 9 33674679 non coding transcript exon variant C/T snv 0.21 1