Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1012068
DEPDC5
0.827 0.160 22 31869917 intron variant T/G snv 0.37 5
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10776934 1.000 0.080 9 135137855 regulatory region variant T/G snv 0.74 1
rs10789491
EFCAB14
1.000 0.080 1 46713638 intron variant A/G snv 0.80 1
rs10814325
RECK
0.827 0.200 9 36036597 upstream gene variant T/A;C;G snv 7
rs10877012
CYP27B1 ; METTL1
0.763 0.280 12 57768302 intron variant G/C;T snv 10
rs1126579
CXCR2
0.776 0.200 2 218136011 3 prime UTR variant T/C snv 0.62 8
rs1127354
ITPA
0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs11506105
EGFR
0.851 0.160 7 55152484 intron variant A/G snv 0.59 4
rs11697186
DDRGK1
1.000 0.080 20 3204477 intron variant A/C;T snv 7.0E-02 1
rs11854484
SLC28A2 ; LOC101928414
0.925 0.120 15 45253280 missense variant C/T snv 0.47 0.45 2
rs11966728 1.000 0.080 6 131955465 intron variant T/C snv 0.26 1
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs1293762
OAS2
1.000 0.080 12 112993031 intron variant T/G snv 0.67 1
rs12952093
LOC101928674
1.000 0.080 17 78367559 intron variant A/C;T snv 1
rs12972991 1.000 0.080 19 39241107 upstream gene variant A/C snv 0.19 1
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs12980602 1.000 0.080 19 39262180 upstream gene variant T/C snv 0.25 1
rs12989760
SH3YL1
0.925 0.120 2 250470 intron variant T/C snv 2
rs1470452230
PAEP
0.925 0.120 9 135561895 missense variant A/C snv 7.0E-06 2