Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 19
rs2075291
APOA5 ; ZPR1
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 15
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 10
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 10
rs12286037
ZPR1
1.000 0.040 11 116781491 intron variant C/T snv 0.11 6
rs2160669
ZPR1
1.000 0.040 11 116776891 3 prime UTR variant C/T snv 0.92 5
rs3741298
ZPR1
11 116786845 intron variant C/T snv 0.73 5
rs2072560
ZPR1 ; APOA5
11 116791110 missense variant T/C snv 0.89 0.94 5
rs11604424
ZPR1
11 116780399 intron variant C/G;T snv 4
rs12285095
ZPR1
11 116787315 non coding transcript exon variant T/G snv 9.8E-02 4
rs201079485
ZPR1 ; APOA5
0.925 0.080 11 116790940 stop gained G/A;T snv 8.0E-05; 4.0E-06 4
rs11823543
ZPR1
11 116778419 3 prime UTR variant G/A snv 0.11 3
rs3135507
ZPR1 ; APOA5
0.925 0.120 11 116790772 missense variant C/T snv 5.0E-02 5.5E-02 3
rs774006043
ZPR1 ; APOA5
0.925 0.080 11 116790561 missense variant C/T snv 3
rs574363219
APOA5 ; ZPR1
1.000 0.040 11 116790427 missense variant C/T snv 1.4E-04 2
rs777046568
APOA5 ; ZPR1
1.000 0.080 11 116790802 frameshift variant G/- del 6.0E-05 7.0E-06 2
rs3741297
ZPR1
11 116786951 intron variant C/T snv 8.6E-03 1.0E-02 2
rs603446
ZPR1
1.000 0.040 11 116783719 intron variant C/T snv 0.33 2
rs121917821
ZPR1 ; APOA5
0.925 0.080 11 116790814 stop gained G/A snv 4.0E-06 2
rs149808404
APOA5 ; ZPR1
11 116790406 stop gained G/A;C snv 4.1E-05; 8.1E-06 1
rs619054
APOA5 ; ZPR1
11 116790097 3 prime UTR variant G/A snv 0.19 0.19 1
rs778114184
APOA5 ; ZPR1
1.000 0.080 11 116790385 missense variant G/A;T snv 2.0E-05 1
rs7118999
BUD13 ; ZPR1
1.000 0.040 11 116774559 3 prime UTR variant C/A;T snv 1
rs10750096
ZPR1
11 116786072 intron variant C/A snv 0.92 1