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
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34 7
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
rs7203984
CETP
16 56965346 intron variant A/C snv 0.31 6
rs7499892
CETP
16 56972678 intron variant C/G;T snv 6
rs9939224
CETP
1.000 0.040 16 56968820 intron variant T/G snv 0.75 6
rs11076175
CETP
16 56972466 intron variant A/G snv 0.20 5
rs11508026
CETP
16 56965416 intron variant C/T snv 0.32 5
rs17231506
CETP
0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 5
rs289714
CETP
16 56973539 intron variant G/A snv 0.76; 4.0E-06 0.70 5
rs11076176
CETP
16 56973534 intron variant T/A;G snv 2.4E-05; 0.22 4
rs12720922
CETP
16 56966973 intron variant G/A snv 0.23 4
rs1532625
CETP
16 56971389 splice region variant C/T snv 0.40 0.34 4
rs708272
CETP
0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 4
rs7205804
CETP
16 56970977 intron variant G/A snv 0.34 4
rs12720900
CETP
16 56977385 non coding transcript exon variant T/C snv 8.9E-04 3
rs2303790
CETP
0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 3
rs289718
CETP
16 56976020 intron variant C/T snv 0.64 3
rs289719
CETP
16 56976029 intron variant T/C snv 0.66 3
rs11076174
CETP
16 56969234 intron variant T/C snv 0.10 2
rs289742
CETP
16 56983850 downstream gene variant C/G snv 0.80 2
rs5880
CETP
0.827 0.040 16 56981179 missense variant G/C snv 5.2E-02 3.7E-02 2
rs5883
CETP
1.000 0.040 16 56973441 synonymous variant C/T snv 5.1E-02 6.6E-02 2
rs9923854
CETP
16 56983090 intron variant T/G snv 0.10 2