Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1617640
EPO
0.742 0.520 7 100719675 upstream gene variant C/A;G;T snv 15
rs138106763
SLC12A9
1.000 0.040 7 100857102 missense variant A/G snv 7.2E-05 1.2E-04 2
rs5030821
VHL
0.827 0.280 3 10149823 missense variant G/A;C;T snv 4.0E-06 8
rs16999593
DNMT1
0.742 0.240 19 10180505 missense variant T/C snv 2.4E-02 9.6E-03 14
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13
rs28362491
LOC105377621 ; NFKB1
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs2001389
SUFU
0.925 0.120 10 102615501 intron variant G/A;C snv 3
rs281432
ICAM1
0.851 0.280 19 10279982 intron variant C/G snv 0.52 12
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs3093030
ICAM4 ; ICAM1
0.925 0.120 19 10286727 non coding transcript exon variant C/T snv 0.34 6
rs1261963959
KIF1B
1 10297069 missense variant G/A snv 4.0E-06 1
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1273593548
PIK3CG
0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs61734277
GCM2
0.882 0.080 6 10874672 missense variant A/C snv 9.1E-03 8.6E-03 5
rs246079
UNG
0.790 0.120 12 109109255 intron variant A/G;T snv 9
rs1332018
GSTM5 ; GSTM3
0.882 0.200 1 109740350 5 prime UTR variant G/T snv 0.64 0.66 6
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs773442580
EGF
0.851 0.080 4 109913367 missense variant T/C;G snv 4.0E-06 7
rs104893859
PITX2
0.925 0.080 4 110618669 missense variant C/G;T snv 3
rs28936409
PITX2
1.000 0.080 4 110621303 missense variant C/A;G;T snv 4.0E-06; 8.0E-06 2
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs201745983
ALDH2
0.752 0.200 12 111783219 missense variant G/A snv 6.8E-05 7.7E-05 14
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116