Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 30
rs3812863
CDX2
1.000 0.080 13 27971131 upstream gene variant G/A snv 0.48 1
rs4769585 1.000 0.080 13 27976441 downstream gene variant C/T snv 0.39 1
rs9257809
OR12D3 ; OR5V1
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 10
rs1202989817
SOD1 ; LOC102724449
0.716 0.360 21 31659813 missense variant T/C;G snv 8.0E-06 7.0E-06 18
rs11631094
SLC12A6
1.000 0.080 15 34332237 intron variant G/C;T snv 1
rs2671828 1.000 0.080 17 35404745 upstream gene variant T/C snv 0.55 1
rs491603
AGO3
1.000 0.080 1 36066715 3 prime UTR variant T/A;C snv 2
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs759412116
ERCC2
0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs1263178238
VSIG10L
0.925 0.080 19 51338047 missense variant T/C snv 2.6E-05 4.9E-05 2
rs6449586 1.000 0.080 5 51339044 intergenic variant C/T snv 0.64 1
rs121434569
EGFR-AS1 ; EGFR
0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs3784262
ALDH1A2
0.882 0.160 15 57960908 intron variant T/A;C snv 6
rs66725070
ALDH1A2
1.000 0.080 15 57975219 intron variant ACAT/- delins 0.35 1
rs2464469
LOC283665 ; ALDH1A2
0.925 0.080 15 58069827 intron variant G/A snv 0.65 2
rs62423175 0.925 0.080 6 61485463 intergenic variant G/A snv 2
rs9918259
CEP72 ; TPPP
0.925 0.080 5 662977 3 prime UTR variant C/T snv 2.1E-03 2
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs4676893 0.882 0.080 3 70868488 intergenic variant A/T snv 0.61 3
rs2687201 0.925 0.080 3 70879779 intergenic variant A/C;G snv 6