Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11880217 1.000 0.080 19 12307980 regulatory region variant C/T snv 0.19 1
rs2431820 1.000 0.080 19 10024608 downstream gene variant T/C snv 8.0E-02 1
rs7259203 1.000 0.080 19 8701483 upstream gene variant T/C;G snv 1
rs1060499841
APOB
1.000 0.080 2 21043911 frameshift variant A/- del 1
rs1135402762
APOB
1.000 0.080 2 21043907 frameshift variant C/- del 1
rs1135402764
APOB
1.000 0.080 2 21019101 frameshift variant T/- delins 1
rs1135402765
APOB
1.000 0.080 2 21012278 frameshift variant G/- delins 1
rs1135402766
APOB
1.000 0.080 2 21004677 splice acceptor variant T/G snv 1
rs1339117465
APOB
1.000 0.080 2 21002271 missense variant A/G snv 4.0E-06 1
rs1382988295
APOB
1.000 0.080 2 21006686 missense variant C/A;T snv 4.0E-06 1
rs1418775778
APOB
1.000 0.080 2 21006144 missense variant C/A;T snv 4.0E-06 1
rs142017360
APOB
1.000 0.080 2 21012217 stop gained G/A snv 7.0E-06 1
rs1442815965
APOB
1.000 0.080 2 21002308 stop gained G/A;T snv 7.0E-06 1
rs1553382295
APOB
1.000 0.080 2 21002202 missense variant A/G snv 1
rs1553382300
APOB
1.000 0.080 2 21002226 missense variant T/G snv 1
rs1553382319
APOB
1.000 0.080 2 21002287 stop gained G/A snv 1
rs1553382325
APOB
1.000 0.080 2 21002292 frameshift variant AT/- del 1
rs1553382326
APOB
1.000 0.080 2 21002296 stop gained G/A snv 1
rs1553385715
APOB
1.000 0.080 2 21025071 frameshift variant TT/- delins 1
rs370481987
APOB
1.000 0.080 2 21006060 missense variant T/C snv 2.0E-05 1.4E-05 1
rs61744153
APOB
1.000 0.080 2 21005391 missense variant G/A;T snv 1.7E-03 1
rs61744288
APOB
1.000 0.080 2 21006088 missense variant A/C;G;T snv 6.4E-04 1
rs747606537
APOB
1.000 0.080 2 21006100 stop gained C/A;T snv 4.0E-06 1
rs750158340
APOB
1.000 0.080 2 21028340 synonymous variant A/G snv 4.0E-06 1
rs759845943
APOB
1.000 0.080 2 21015387 missense variant C/G;T snv 4.0E-06 1