Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1223231582
PRSS1
0.677 0.280 7 142750639 missense variant A/G snv 7.0E-06 24
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
rs104894365
KRAS
0.827 0.320 12 25245345 missense variant C/T snv 9
rs756322971
CASR
0.763 0.240 3 122284955 missense variant C/A;G 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
rs886037774
LPL
0.882 0.120 8 19955993 missense variant T/C snv 7
rs886037775
LPL
0.882 0.120 8 19960948 missense variant A/T snv 7
rs12688220
MORC4
0.827 0.200 X 107001537 upstream gene variant C/T snv 0.19 5
rs42490
RIPK2
0.882 0.160 8 89766285 intron variant G/A snv 0.60 5
rs7057398
MORC4 ; RIPPLY1 ; CLDN2
0.827 0.080 X 106901299 intron variant T/C snv 0.41 5
rs111033567
PRSS1
0.882 0.040 7 142750582 missense variant A/G snv 3
rs12008279
MORC4 ; CLDN2
0.882 0.080 X 106917472 intron variant A/G;T snv 3
rs12014762
MORC4
0.882 0.080 X 106940440 intron variant C/T snv 0.14 3
rs1335550286
APOE
1.000 0.040 19 44909005 missense variant G/A snv 7.0E-06 2
rs2647087 1.000 0.040 6 32713272 upstream gene variant A/C snv 0.29 2
rs2995271
LOC101929279
0.925 0.040 10 30230903 regulatory region variant C/T snv 0.64 2
rs397507442
PRSS1
0.925 0.040 7 142750579 missense variant A/G snv 2
rs4409525
MORC4
0.925 0.040 X 106897095 intron variant G/A snv 0.28 2
rs4437130 1.000 0.040 3 2035283 intergenic variant G/A snv 0.12 2
rs62561366 1.000 0.040 9 95555669 intergenic variant A/T snv 3.9E-02 2
rs72558408
OTC
0.925 0.160 X 38403681 missense variant C/T snv 2
rs756271986
PRSS2
0.925 0.040 7 142773430 missense variant GC/AT mnv 2