Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs379742 1.000 0.040 X 106250703 intergenic variant G/A snv 0.17 1
rs62228256
LINC01429
1.000 0.040 20 51837908 intron variant C/T snv 2.7E-02 1
rs5917027
MORC4 ; CLDN2
1.000 0.040 X 106919404 intron variant C/A;T snv 1
rs145867820
PRSS1
1.000 0.040 7 142751775 missense variant C/T snv 1
rs13228878
PRSS2
1.000 0.040 7 142765617 intron variant G/A snv 0.51 1
rs139232307
PRSS2
1.000 0.040 7 142773300 missense variant G/A snv 1.4E-05 1
rs34708521
SPEF2
1.000 0.040 5 35670201 missense variant G/A;T snv 0.10; 4.0E-06 1
rs515726208
SPINK1
1.000 0.040 5 147824702 missense variant G/A snv 3.2E-05 1.4E-05 1
rs2647087 1.000 0.040 6 32713272 upstream gene variant A/C snv 0.29 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
rs574363219
APOA5 ; ZPR1
1.000 0.040 11 116790427 missense variant C/T snv 1.4E-04 2
rs1335550286
APOE
1.000 0.040 19 44909005 missense variant G/A snv 7.0E-06 2
rs199695765
CPA2
0.925 0.160 7 130269008 stop gained C/T snv 8.8E-05 1.3E-04 2
rs1451011538
CRISPLD2
0.925 0.080 16 84838647 missense variant T/A snv 4.0E-06 2
rs142560329
CTRC
0.925 0.040 1 15445703 missense variant C/T snv 9.9E-05 2.2E-04 2
rs2995271
LOC101929279
0.925 0.040 10 30230903 regulatory region variant C/T snv 0.64 2
rs4409525
MORC4
0.925 0.040 X 106897095 intron variant G/A snv 0.28 2
rs72558408
OTC
0.925 0.160 X 38403681 missense variant C/T snv 2
rs111033564
PRSS1
0.925 0.040 7 142751808 splice donor variant G/A snv 3.6E-05 9.8E-05 2
rs199422123
PRSS1
0.925 0.040 7 142751934 missense variant G/A;T snv 2.0E-05 2
rs397507442
PRSS1
0.925 0.040 7 142750579 missense variant A/G 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
rs190853081
APOE
0.925 0.080 19 44909083 missense variant G/A snv 2.0E-04 5.6E-05 3