Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12720873
CETP
16 56972160 intron variant G/A;C snv 2
rs11076175
CETP
16 56972466 intron variant A/G snv 0.20 5
rs7499892
CETP
16 56972678 intron variant C/G;T snv 6
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
rs11076176
CETP
16 56973534 intron variant T/A;G snv 2.4E-05; 0.22 4
rs289714
CETP
16 56973539 intron variant G/A snv 0.76; 4.0E-06 0.70 5
rs158477
CETP
16 56973698 intron variant G/A snv 0.49 2
rs158480
CETP
16 56974315 intron variant G/A snv 0.78 2
rs289715
CETP
16 56974596 intron variant A/C;T snv 2
rs289716
CETP
16 56975464 intron variant T/A snv 0.63 2
rs289717
CETP
16 56975476 intron variant G/A;T snv 2
rs736274
CETP
16 56975857 intron variant T/A snv 8.7E-02 2
rs289718
CETP
16 56976020 intron variant C/T snv 0.64 3
rs289719
CETP
16 56976029 intron variant T/C snv 0.66 3
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
rs12708980
CETP
16 56978467 intron variant T/G snv 0.36 2
rs12720889
CETP
16 56978651 intron variant A/T snv 0.27 2
rs4784745
CETP
16 56980963 intron variant A/C;G snv 2
rs5880
CETP
0.827 0.040 16 56981179 missense variant G/C snv 5.2E-02 3.7E-02 2
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 3
rs9923854
CETP
16 56983090 intron variant T/G snv 0.10 2
rs2303790
CETP
0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 3