Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs533617
APOB
2 21011100 missense variant T/C snv 3.1E-02 2.9E-02 6
rs10199768
APOB
2 21021128 intron variant G/T snv 0.35 5
rs1041968
APOB
2 21009932 synonymous variant G/A snv 0.39 0.38 4
rs12691202
APOB
2 21026844 missense variant C/T snv 2.7E-02 2.7E-02 3
rs934197
APOB
2 21044589 upstream gene variant G/A snv 0.25 3
rs12720828
APOB
2 21018872 intron variant C/T snv 0.13 3
rs2854725
APOB
2 21014914 intron variant T/A;G snv 3
rs12720826
APOB
2 21042823 intron variant T/C snv 3.8E-02 3
rs520354
APOB
2 21036740 intron variant A/G snv 0.39 3
rs12720838
APOB
2 21024339 3 prime UTR variant C/T snv 0.14 3
rs531819
APOB
2 21040767 intron variant T/G snv 0.83 3
rs1800481
APOB
2 21044338 upstream gene variant A/G snv 0.82 3
rs570877
APOB
2 21028168 intron variant T/G snv 0.87 3
rs597331
APOB
2 21039555 intron variant G/A;T snv 3
rs12713956
APOB
2 21018633 intron variant A/G snv 0.14 3
rs550619
APOB
2 21037729 intron variant G/A snv 0.86 3
rs1800479
APOB
2 21004511 intron variant C/G snv 0.16 0.17 3
rs3749054
APOB
2 21014366 intron variant A/T snv 0.13 3
rs12720847
APOB
2 21012503 missense variant G/A;C snv 5.1E-03 1
rs3791980
APOB
2 21022457 intron variant G/T snv 0.70 1
rs11126598
APOB
2 21017492 intron variant A/G snv 0.73 1
rs11680233
APOB
2 21017159 intron variant A/C;T snv 1
rs5742904
APOB
0.689 0.280 2 21006288 missense variant C/A;T snv 2.8E-04 7.3E-04 3
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 7
rs1042031
APOB
0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 3