Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
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
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs5275
PTGS2
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs1223231582
PRSS1
0.677 0.280 7 142750639 missense variant A/G snv 7.0E-06 24
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs111033566
PRSS1
0.742 0.280 7 142750600 missense variant A/C;T snv 11
rs267606982
PRSS1
0.742 0.120 7 142751938 missense variant GC/AT mnv 11
rs4251961
IL1RN
0.763 0.200 2 113116890 intron variant T/C snv 0.29 10
rs10273639
PRSS1
0.776 0.280 7 142749077 upstream gene variant T/A;C snv 9
rs61734659
PRSS2
0.790 0.160 7 142774035 missense variant G/A snv 1.4E-02 8
rs748405415
PRSS2
0.790 0.160 7 142773993 stop gained G/A;T snv 8
rs773891125
LPL
0.827 0.120 8 19955896 frameshift variant CT/- delins 6
rs12688220
MORC4
0.827 0.200 X 107001537 upstream gene variant C/T snv 0.19 5
rs7057398
MORC4 ; RIPPLY1 ; CLDN2
0.827 0.080 X 106901299 intron variant T/C snv 0.41 5
rs5029924
TNFAIP3 ; WAKMAR2
0.851 0.200 6 137866361 intron variant C/T snv 0.13 4
rs1451659304
LMF1
1.000 0.040 16 868990 missense variant A/C snv 2
rs1490931437
TP53
0.925 0.120 17 7673260 missense variant G/A snv 2
rs752688735
PRSS1
0.925 0.040 7 142752547 missense variant G/A snv 2
rs756271986
PRSS2
0.925 0.040 7 142773430 missense variant GC/AT mnv 2
rs764176833
PRSS2
0.925 0.040 7 142773430 missense variant G/A snv 2