Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs5275
PTGS2
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
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
rs78655421
CFTR
0.716 0.240 7 117530975 missense variant G/A;C;T snv 1.5E-03; 1.2E-05 18
rs111033565
PRSS1
0.742 0.120 7 142751938 missense variant G/A snv 1.2E-05 11
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
rs10273639
PRSS1
0.776 0.280 7 142749077 upstream gene variant T/A;C snv 9
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
rs1805017
PLA2G7
0.851 0.240 6 46716485 missense variant C/A;T snv 4.0E-06; 0.31 5
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
rs497078
CTRC
0.925 0.040 1 15440540 synonymous variant C/A;T snv 3.7E-03; 9.1E-02 2
rs5707
REN
1.000 0.040 1 204160543 intron variant A/C;G;T snv 0.25; 2.0E-05; 1.2E-05 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
rs1132312
CASP9
1.000 0.040 1 15518120 missense variant A/C;G;T snv 0.53 1
rs139635080
UBE2R2-AS1 ; PRSS3
1.000 0.040 9 33798602 missense variant G/A snv 1
rs142907823
TNFRSF1B
1.000 0.040 1 12188800 missense variant C/T snv 4.0E-06 1
rs146966861
UBE2R2-AS1 ; PRSS3
1.000 0.040 9 33797993 missense variant G/A snv 1
rs778574118
CASP7
1.000 0.040 10 113721138 missense variant A/G snv 4.0E-06 1
rs1223231582
PRSS1
0.677 0.280 7 142750639 missense variant A/G snv 7.0E-06 24