Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs289742
CETP
16 56983850 downstream gene variant C/G snv 0.80 2
rs289743
CETP
16 56983884 downstream gene variant G/A;C;T snv 2
rs289744
CETP
16 56984190 downstream gene variant G/T snv 0.61 2
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 7
rs17231506
CETP
0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 5
rs12720918
CETP
16 56960300 upstream gene variant T/C snv 0.26 3
rs4783961
CETP
0.851 0.320 16 56960982 upstream gene variant G/A snv 0.48 0.47 3
rs12447839
CETP
16 56960023 upstream gene variant C/A;G;T snv 2
rs12447924
CETP
1.000 16 56960280 upstream gene variant C/T snv 0.76 2
rs17231520
CETP
0.851 0.240 16 56961915 upstream gene variant G/A snv 2.1E-02 2
rs1800776
CETP
16 56961322 upstream gene variant C/A snv 5.2E-02 5.5E-02 2
rs4783962
CETP
16 56961126 upstream gene variant T/C snv 0.80 2
rs711752
CETP
1.000 0.040 16 56962299 splice region variant G/A;C snv 6
rs1532625
CETP
16 56971389 splice region variant C/T snv 0.40 0.34 4
rs1801706
CETP
1.000 0.040 16 56983750 3 prime UTR variant G/A snv 0.17 2
rs5883
CETP
1.000 0.040 16 56973441 synonymous variant C/T snv 5.1E-02 6.6E-02 2
rs4784744
CETP
16 56977273 non coding transcript exon variant G/A snv 0.30 3
rs291044
CETP
16 56977540 non coding transcript exon variant G/A snv 0.28 2
rs891144
CETP
16 56978024 non coding transcript exon variant C/T snv 7.3E-02 2
rs2303790
CETP
0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 3
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 3
rs1800777
CETP
0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 2
rs5880
CETP
0.827 0.040 16 56981179 missense variant G/C snv 5.2E-02 3.7E-02 2
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 8
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34 7