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: rs118204078
rs118204078
LPL
2 0.925 0.080 8 19960935 missense variant C/G snv 0.010 1.000 1 2015 2015
dbSNP: rs2020927
rs2020927
ABCA1
1 1.000 9 104790904 intron variant A/G snv 0.18 0.24 0.010 1.000 1 2009 2009
dbSNP: rs2281997
rs2281997
ENHO
5 0.882 0.240 9 34521869 intron variant T/A;C snv 0.010 1.000 1 2018 2018
dbSNP: rs268
rs268
LPL
41 0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 0.010 1.000 1 2015 2015
dbSNP: rs3135506
rs3135506
APOA5
26 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 0.010 1.000 1 2015 2015
dbSNP: rs328
rs328
LPL
19 0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 0.010 1.000 1 2015 2015
dbSNP: rs4149263
rs4149263
ABCA1
2 0.925 0.080 9 104915008 intron variant A/G snv 0.18 0.010 1.000 1 2009 2009
dbSNP: rs662799
rs662799
APOA5
33 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.010 1.000 1 2015 2015
dbSNP: rs7903146
rs7903146
TCF7L2
93 0.554 0.680 10 112998590 intron variant C/G;T snv 0.010 1.000 1 2009 2009