Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1049305
AQP1
0.925 0.160 7 30924207 3 prime UTR variant G/C snv 0.52 4
rs510432
ATG5
0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 11
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 11
rs367956522
ATP7B
0.851 0.240 13 51949798 splice acceptor variant T/C snv 2.4E-05 7.7E-05 7
rs10146249
ATXN3
1.000 0.080 14 92074996 intron variant C/A snv 0.29 1
rs7158733
ATXN3
1.000 0.080 14 92070879 stop gained G/A;T snv 1.2E-05; 0.27 1
rs2679757
AZIN1
0.925 0.080 8 102858590 intron variant A/G snv 0.37 2
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs2303015
CALCOCO2
0.851 0.160 17 48852546 missense variant T/C snv 7.4E-02 0.12 4
rs4646038
CASP9
0.925 0.080 1 15506705 intron variant C/T snv 7.0E-06 2
rs769217
CAT
0.742 0.440 11 34461361 synonymous variant C/T snv 0.25 0.22 12
rs4656942
CD244
0.851 0.160 1 160861258 intron variant G/A;C;T snv 4
rs485618
CD244
0.851 0.160 1 160830690 3 prime UTR variant T/A;C;G snv 0.54 4
rs13347
CD44
0.763 0.320 11 35231725 3 prime UTR variant C/A;T snv 12
rs75961395
CFTR
0.763 0.280 7 117509123 missense variant G/A;T snv 4.0E-05 10
rs1227756
COL13A1
0.925 0.080 10 69828748 intron variant G/A;C snv 2
rs3106796
COL3A1 ; LOC105373791
0.882 0.160 2 188985047 non coding transcript exon variant A/G snv 0.35 3
rs3811381
CR1
0.763 0.240 1 207616743 missense variant C/A;G snv 8.0E-06; 0.24 11
rs2274567
CR1
0.776 0.400 1 207580276 missense variant A/G snv 0.25 0.21 10
rs887304
CRACR2A
0.925 0.080 12 3648382 3 prime UTR variant T/C snv 0.77 2
rs4074
CXCL1
0.827 0.200 4 73870427 intron variant A/G snv 0.46 6
rs2234671
CXCR1
0.807 0.240 2 218164385 missense variant C/G snv 9.1E-02 0.11 7
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs4646437
CYP3A4
0.827 0.200 7 99767460 intron variant G/A snv 0.30 8
rs2710833
DDX60L ; LOC107986198
0.925 0.080 4 168488807 intron variant T/A;C snv 2