Gene: CETP ×
Source: ALL
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: rs12720922
rs12720922
CETP
6 16 56966973 intron variant G/A snv 0.23 0.700 1.000 1 2012 2012
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: rs1801706
rs1801706
CETP
3 1.000 0.040 16 56983750 3 prime UTR variant G/A snv 0.17 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
3 16 56983850 downstream gene variant C/G snv 0.80 0.700 1.000 1 2012 2012
dbSNP: rs289743
rs289743
CETP
2 16 56983884 downstream gene variant G/A;C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs289744
rs289744
CETP
2 16 56984190 downstream gene variant G/T snv 0.61 0.700 1.000 1 2011 2011
dbSNP: rs291044
rs291044
CETP
2 16 56977540 non coding transcript exon variant G/A snv 0.28 0.700 1.000 1 2012 2012
dbSNP: rs4587963
rs4587963
CETP
2 16 56963457 intron variant A/T snv 0.79 0.700 1.000 1 2012 2012
dbSNP: rs4783962
rs4783962
CETP
2 16 56961126 upstream gene variant T/C snv 0.80 0.700 1.000 1 2012 2012
dbSNP: rs4784745
rs4784745
CETP
2 16 56980963 intron variant A/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs708273
rs708273
CETP
2 16 56966037 intron variant A/G snv 0.76 0.700 1.000 1 2012 2012
dbSNP: rs7203984
rs7203984
CETP
7 16 56965346 intron variant A/C snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs7205804
rs7205804
CETP
6 16 56970977 intron variant G/A snv 0.34 0.700 1.000 1 2008 2008
dbSNP: rs736274
rs736274
CETP
2 16 56975857 intron variant T/A snv 8.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs820299
rs820299
CETP
2 16 56966372 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs891144
rs891144
CETP
2 16 56978024 non coding transcript exon variant C/T snv 7.3E-02 0.700 1.000 1 2012 2012