Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 8
rs12597002
CETP
1.000 16 56968492 intron variant C/A snv 0.25 2
rs12720922
CETP
16 56966973 intron variant G/A snv 0.23 4
rs11076175
CETP
16 56972466 intron variant A/G snv 0.20 5
rs1801706
CETP
1.000 0.040 16 56983750 3 prime UTR variant G/A snv 0.17 2
rs9923854
CETP
16 56983090 intron variant T/G snv 0.10 2
rs11076174
CETP
16 56969234 intron variant T/C snv 0.10 2
rs118146573
CETP
16 56967026 intron variant G/A snv 9.4E-02 1
rs736274
CETP
16 56975857 intron variant T/A snv 8.7E-02 2
rs891144
CETP
16 56978024 non coding transcript exon variant C/T snv 7.3E-02 2
rs9930761
CETP
16 56973280 intron variant T/C snv 5.9E-02 7.3E-02 2
rs5883
CETP
1.000 0.040 16 56973441 synonymous variant C/T snv 5.1E-02 6.6E-02 2
rs1800776
CETP
16 56961322 upstream gene variant C/A snv 5.2E-02 5.5E-02 2
rs5880
CETP
0.827 0.040 16 56981179 missense variant G/C snv 5.2E-02 3.7E-02 2
rs1800777
CETP
0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 2
rs17231520
CETP
0.851 0.240 16 56961915 upstream gene variant G/A snv 2.1E-02 2
rs2303790
CETP
0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 3
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 7
rs711752
CETP
1.000 0.040 16 56962299 splice region variant G/A;C snv 6
rs7499892
CETP
16 56972678 intron variant C/G;T snv 6
rs17231506
CETP
0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 5
rs11076176
CETP
16 56973534 intron variant T/A;G snv 2.4E-05; 0.22 4
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 3
rs12447839
CETP
16 56960023 upstream gene variant C/A;G;T snv 2
rs12720873
CETP
16 56972160 intron variant G/A;C snv 2