Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs999885
AP4M1 ; MCM7
0.925 0.120 7 100103553 intron variant G/A snv 0.56 0.46 3
rs12438080
CERS3
1.000 0.080 15 100541858 intron variant A/C snv 0.50 2
rs2295660
DLK1
1.000 0.080 14 100734443 synonymous variant T/C snv 1.1E-02 1.2E-02 1
rs2305160
NPAS2 ; NPAS2-AS1
0.776 0.200 2 100974842 missense variant A/G snv 0.71 0.75 9
rs4919510
SEMA4G ; MIR608 ; MRPL43
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs1053096
NPAS2
1.000 0.080 2 100996153 3 prime UTR variant T/C snv 0.61 1
rs16405
BTRC
0.882 0.120 10 101553963 3 prime UTR variant AACAGTGGA/- del 0.31 4
rs3821204
IL18R1 ; IL1RL1
0.807 0.160 2 102343821 3 prime UTR variant C/G snv 0.21 6
rs28362491
LOC105377621 ; NFKB1
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs750521832
MMP8
0.732 0.200 11 102718452 missense variant A/G snv 4.0E-06 14
rs743572
CYP17A1
0.672 0.360 10 102837395 5 prime UTR variant A/G;T snv 0.40; 8.1E-06 24
rs751402
ERCC5 ; BIVM-ERCC5
0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs873601
BIVM-ERCC5 ; ERCC5
0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25
rs5945919
LINC00630
1.000 0.080 X 102963359 intergenic variant A/G snv 0.20 1
rs17401966
KIF1B
0.790 0.280 1 10325413 intron variant A/G snv 0.24 7
rs3748578
KIF1B ; LOC105376725
1.000 0.080 1 10360860 intron variant G/A snv 0.29 1
rs745564626
XRCC3 ; KLC1
0.752 0.280 14 103699003 missense variant C/G;T snv 4.3E-05 14
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1297812518
LOC112268131 ; KLC1 ; XRCC3
0.763 0.160 14 103707168 missense variant G/A snv 1.3E-05 1.4E-05 9
rs1799794
XRCC3 ; KLC1
0.763 0.320 14 103712930 splice region variant T/C snv 0.22 12
rs157077
GSTO2
1.000 0.080 10 104278136 intron variant T/C snv 0.45 0.53 3
rs7085725
GSTO2
1.000 0.080 10 104300451 3 prime UTR variant T/C snv 9.9E-02 1
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs2494752
AKT1
0.790 0.120 14 104797271 upstream gene variant A/G snv 0.85 10