Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs5744174
TLR5
0.742 0.360 1 223111186 missense variant A/G snv 0.39 0.34 13
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
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
rs2843403
MMEL1
0.882 0.200 1 2597658 intron variant T/C snv 0.54 3
rs56073403
AGT
0.882 0.160 1 230710009 missense variant T/C snv 7.2E-04 6.8E-04 3
rs7536540
MIR101-1 ; MIR3671 ; JAK1
0.882 0.160 1 65058899 intron variant C/G;T snv 0.65 3
rs4646038
CASP9
0.925 0.080 1 15506705 intron variant C/T snv 7.0E-06 2
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs2292832
MIR149 ; GPC1 ; LOC100130449
0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs2241880
SCARNA5 ; ATG16L1
0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs10204525
PDCD1
0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 20
rs2287622
ABCB11
0.724 0.240 2 168973818 missense variant A/C;G;T snv 0.57 16
rs2241883
FABP1
0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 14