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: rs7499892
rs7499892
CETP
6 16 56972678 intron variant C/G;T snv 0.800 1.000 4 2011 2019
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: rs4784744
rs4784744
CETP
3 16 56977273 non coding transcript exon variant G/A snv 0.30 0.700 1.000 2 2011 2012
dbSNP: rs11076174
rs11076174
CETP
2 16 56969234 intron variant T/C snv 0.10 0.800 1.000 1 2012 2019
dbSNP: rs11076175
rs11076175
CETP
5 16 56972466 intron variant A/G snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs11508026
rs11508026
CETP
5 16 56965416 intron variant C/T snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs12447839
rs12447839
CETP
2 16 56960023 upstream gene variant C/A;G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs12447924
rs12447924
CETP
2 1.000 16 56960280 upstream gene variant C/T snv 0.76 0.700 1.000 1 2012 2012
dbSNP: rs12597002
rs12597002
CETP
2 1.000 16 56968492 intron variant C/A snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs12708980
rs12708980
CETP
2 16 56978467 intron variant T/G snv 0.36 0.800 1.000 1 2011 2019
dbSNP: rs12720873
rs12720873
CETP
2 16 56972160 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs12720889
rs12720889
CETP
2 16 56978651 intron variant A/T snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs12720918
rs12720918
CETP
3 16 56960300 upstream gene variant T/C snv 0.26 0.700 1.000 1 2012 2012
dbSNP: rs12720922
rs12720922
CETP
4 16 56966973 intron variant G/A snv 0.23 0.800 1.000 1 2012 2019
dbSNP: rs1532625
rs1532625
CETP
4 16 56971389 splice region variant C/T snv 0.40 0.34 0.700 1.000 1 2012 2012
dbSNP: rs158477
rs158477
CETP
2 16 56973698 intron variant G/A snv 0.49 0.700 1.000 1 2012 2012
dbSNP: rs158480
rs158480
CETP
2 16 56974315 intron variant G/A snv 0.78 0.700 1.000 1 2012 2012
dbSNP: rs1800776
rs1800776
CETP
2 16 56961322 upstream gene variant C/A snv 5.2E-02 5.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs289714
rs289714
CETP
5 16 56973539 intron variant G/A snv 0.76; 4.0E-06 0.70 0.700 1.000 1 2012 2012
dbSNP: rs289715
rs289715
CETP
2 16 56974596 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs289716
rs289716
CETP
2 16 56975464 intron variant T/A snv 0.63 0.700 1.000 1 2012 2012
dbSNP: rs289717
rs289717
CETP
2 16 56975476 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs289718
rs289718
CETP
3 16 56976020 intron variant C/T snv 0.64 0.700 1.000 1 2012 2012
dbSNP: rs289719
rs289719
CETP
3 16 56976029 intron variant T/C snv 0.66 0.700 1.000 1 2012 2012
dbSNP: rs289742
rs289742
CETP
2 16 56983850 downstream gene variant C/G snv 0.80 0.800 1.000 1 2012 2019