Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs777418530
CRISPLD2
0.763 0.120 16 84845883 missense variant A/G snv 4.0E-06 7.0E-06 10
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
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
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
rs1805017
PLA2G7
0.851 0.240 6 46716485 missense variant C/A;T snv 4.0E-06; 0.31 5
rs1052571
CASP9
0.882 0.080 1 15524118 missense variant G/A snv 0.50 0.59 4
rs5029924
TNFAIP3 ; WAKMAR2
0.851 0.200 6 137866361 intron variant C/T snv 0.13 4
rs145657341
LPL
0.925 0.120 8 19951811 missense variant G/A snv 1.7E-04 7.0E-05 3
rs497078
CTRC
0.925 0.040 1 15440540 synonymous variant C/A;T snv 3.7E-03; 9.1E-02 2
rs1451659304
LMF1
1.000 0.040 16 868990 missense variant A/C 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
rs5707
REN
1.000 0.040 1 204160543 intron variant A/C;G;T snv 0.25; 2.0E-05; 1.2E-05 2
rs1490931437
TP53
0.925 0.120 17 7673260 missense variant G/A snv 2
rs778574118
CASP7
1.000 0.040 10 113721138 missense variant A/G snv 4.0E-06 1
rs1132312
CASP9
1.000 0.040 1 15518120 missense variant A/C;G;T snv 0.53 1
rs5743795
TLR6 ; TLR1
1.000 0.040 4 38830874 intron variant C/T snv 0.14 1
rs142907823
TNFRSF1B
1.000 0.040 1 12188800 missense variant C/T snv 4.0E-06 1
rs139635080
UBE2R2-AS1 ; PRSS3
1.000 0.040 9 33798602 missense variant G/A snv 1