Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs12720918
CETP
16 56960300 upstream gene variant T/C snv 0.26 3
rs17231506
CETP
0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 5
rs4783961
CETP
0.851 0.320 16 56960982 upstream gene variant G/A snv 0.48 0.47 3
rs4783962
CETP
16 56961126 upstream gene variant T/C snv 0.80 2
rs1800776
CETP
16 56961322 upstream gene variant C/A snv 5.2E-02 5.5E-02 2
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 7
rs17231520
CETP
0.851 0.240 16 56961915 upstream gene variant G/A snv 2.1E-02 2
rs711752
CETP
1.000 0.040 16 56962299 splice region variant G/A;C snv 6
rs708272
CETP
0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 4
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 8
rs4587963
CETP
16 56963457 intron variant A/T snv 0.79 2
rs7203984
CETP
16 56965346 intron variant A/C snv 0.31 6
rs11508026
CETP
16 56965416 intron variant C/T snv 0.32 5
rs708273
CETP
16 56966037 intron variant A/G snv 0.76 2
rs820299
CETP
16 56966372 intron variant G/A;C snv 2
rs12720922
CETP
16 56966973 intron variant G/A snv 0.23 4
rs118146573
CETP
16 56967026 intron variant G/A snv 9.4E-02 1
rs12597002
CETP
1.000 16 56968492 intron variant C/A snv 0.25 2
rs9939224
CETP
1.000 0.040 16 56968820 intron variant T/G snv 0.75 6
rs11076174
CETP
16 56969234 intron variant T/C snv 0.10 2
rs7205804
CETP
16 56970977 intron variant G/A snv 0.34 4
rs1532625
CETP
16 56971389 splice region variant C/T snv 0.40 0.34 4
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34 7