Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1052571
CASP9
0.882 0.080 1 15524118 missense variant G/A snv 0.50 0.59 4
rs5275
PTGS2
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs145657341
LPL
0.925 0.120 8 19951811 missense variant G/A snv 1.7E-04 7.0E-05 3
rs773891125
LPL
0.827 0.120 8 19955896 frameshift variant CT/- delins 6
rs371282890
LPL
0.827 0.120 8 19955900 missense variant C/G snv 1.1E-04 6.3E-05 6
rs5707
REN
1.000 0.040 1 204160543 intron variant A/C;G;T snv 0.25; 2.0E-05; 1.2E-05 2
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs146966861
UBE2R2-AS1 ; PRSS3
1.000 0.040 9 33797993 missense variant G/A snv 1
rs139635080
UBE2R2-AS1 ; PRSS3
1.000 0.040 9 33798602 missense variant G/A snv 1
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs5743795
TLR6 ; TLR1
1.000 0.040 4 38830874 intron variant C/T snv 0.14 1
rs76863441
PLA2G7
0.672 0.440 6 46709361 missense variant C/A snv 4.5E-03 1.3E-03 25
rs1805017
PLA2G7
0.851 0.240 6 46716485 missense variant C/A;T snv 4.0E-06; 0.31 5
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
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1490931437
TP53
0.925 0.120 17 7673260 missense variant G/A snv 2
rs121912654
TP53
0.683 0.400 17 7675143 missense variant C/A;T snv 4.0E-05 21
rs9904341
BIRC5
0.695 0.280 17 78214286 5 prime UTR variant G/A;C;T snv 0.38; 4.8E-06 20
rs777418530
CRISPLD2
0.763 0.120 16 84845883 missense variant A/G snv 4.0E-06 7.0E-06 10