Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
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
rs371282890
LPL
0.827 0.120 8 19955900 missense variant C/G snv 1.1E-04 6.3E-05 6
rs773891125
LPL
0.827 0.120 8 19955896 frameshift variant CT/- delins 6
rs145657341
LPL
0.925 0.120 8 19951811 missense variant G/A snv 1.7E-04 7.0E-05 3
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs139635080
UBE2R2-AS1 ; PRSS3
1.000 0.040 9 33798602 missense variant G/A snv 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
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs777418530
CRISPLD2
0.763 0.120 16 84845883 missense variant A/G snv 4.0E-06 7.0E-06 10
rs1451659304
LMF1
1.000 0.040 16 868990 missense variant A/C 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
rs1490931437
TP53
0.925 0.120 17 7673260 missense variant G/A snv 2
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs12688220
MORC4
0.827 0.200 X 107001537 upstream gene variant C/T snv 0.19 5