Gene: CETP ×
Source: GWASDB ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1800775
rs1800775
CETP
7 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 0.800 1.000 5 2007 2019
dbSNP: rs1532624
rs1532624
CETP
7 0.851 0.160 16 56971567 intron variant C/A snv 0.34 0.800 1.000 4 2009 2019
dbSNP: rs5880
rs5880
CETP
2 0.827 0.040 16 56981179 missense variant G/C snv 5.2E-02 3.7E-02 0.800 1.000 4 2008 2019
dbSNP: rs7499892
rs7499892
CETP
6 16 56972678 intron variant C/G;T snv 0.800 1.000 4 2011 2019
dbSNP: rs1864163
rs1864163
CETP
8 0.882 0.120 16 56963321 intron variant G/A snv 0.26 0.800 1.000 3 2008 2019
dbSNP: rs4783961
rs4783961
CETP
3 0.851 0.320 16 56960982 upstream gene variant G/A snv 0.48 0.47 0.800 1.000 3 2012 2019
dbSNP: rs711752
rs711752
CETP
6 1.000 0.040 16 56962299 splice region variant G/A;C snv 0.800 1.000 3 2008 2016
dbSNP: rs17231506
rs17231506
CETP
5 0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 0.800 1.000 2 2012 2019
dbSNP: rs17231520
rs17231520
CETP
2 0.851 0.240 16 56961915 upstream gene variant G/A snv 2.1E-02 0.800 1.000 2 2012 2019
dbSNP: rs5883
rs5883
CETP
2 1.000 0.040 16 56973441 synonymous variant C/T snv 5.1E-02 6.6E-02 0.800 1.000 2 2012 2019
dbSNP: rs11076174
rs11076174
CETP
2 16 56969234 intron variant T/C snv 0.10 0.800 1.000 1 2012 2019
dbSNP: rs12708980
rs12708980
CETP
2 16 56978467 intron variant T/G snv 0.36 0.800 1.000 1 2011 2019
dbSNP: rs12720922
rs12720922
CETP
4 16 56966973 intron variant G/A snv 0.23 0.800 1.000 1 2012 2019
dbSNP: rs1801706
rs1801706
CETP
2 1.000 0.040 16 56983750 3 prime UTR variant G/A snv 0.17 0.800 1.000 1 2012 2018
dbSNP: rs289742
rs289742
CETP
2 16 56983850 downstream gene variant C/G snv 0.80 0.800 1.000 1 2012 2019
dbSNP: rs7205804
rs7205804
CETP
4 16 56970977 intron variant G/A snv 0.34 0.800 1.000 1 2008 2019
dbSNP: rs820299
rs820299
CETP
2 16 56966372 intron variant G/A;C snv 0.800 1.000 1 2012 2018
dbSNP: rs9923854
rs9923854
CETP
2 16 56983090 intron variant T/G snv 0.10 0.800 1.000 1 2012 2019
dbSNP: rs9939224
rs9939224
CETP
6 1.000 0.040 16 56968820 intron variant T/G snv 0.75 0.800 1.000 1 2012 2018
dbSNP: rs5882
rs5882
CETP
3 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.700 1.000 3 2008 2012
dbSNP: rs11076176
rs11076176
CETP
4 16 56973534 intron variant T/A;G snv 2.4E-05; 0.22 0.700 1.000 2 2012 2012
dbSNP: rs1800777
rs1800777
CETP
2 0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 0.700 1.000 2 2008 2012
dbSNP: rs4784744
rs4784744
CETP
3 16 56977273 non coding transcript exon variant G/A snv 0.30 0.700 1.000 2 2011 2012
dbSNP: rs708272
rs708272
CETP
4 0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 0.700 1.000 2 2011 2012
dbSNP: rs11076175
rs11076175
CETP
5 16 56972466 intron variant A/G snv 0.20 0.700 1.000 1 2012 2012