Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs289717
CETP
16 56975476 intron variant G/A;T snv 2
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
rs291044
CETP
16 56977540 non coding transcript exon variant G/A snv 0.28 2
rs4587963
CETP
16 56963457 intron variant A/T snv 0.79 2
rs4783962
CETP
16 56961126 upstream gene variant T/C snv 0.80 2
rs4784745
CETP
16 56980963 intron variant A/C;G snv 2
rs708273
CETP
16 56966037 intron variant A/G snv 0.76 2
rs736274
CETP
16 56975857 intron variant T/A snv 8.7E-02 2
rs820299
CETP
16 56966372 intron variant G/A;C snv 2
rs891144
CETP
16 56978024 non coding transcript exon variant C/T snv 7.3E-02 2
rs9923854
CETP
16 56983090 intron variant T/G snv 0.10 2
rs9930761
CETP
16 56973280 intron variant T/C snv 5.9E-02 7.3E-02 2
rs118146573
CETP
16 56967026 intron variant G/A snv 9.4E-02 1
rs711752
CETP
1.000 0.040 16 56962299 splice region variant G/A;C snv 6
rs9939224
CETP
1.000 0.040 16 56968820 intron variant T/G snv 0.75 6
rs17231506
CETP
0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 5
rs1801706
CETP
1.000 0.040 16 56983750 3 prime UTR variant G/A snv 0.17 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
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
rs17231520
CETP
0.851 0.240 16 56961915 upstream gene variant G/A snv 2.1E-02 2