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: rs2083637
rs2083637 		6 0.925 0.080 8 20007664 intergenic variant A/G snv 0.25 0.800 1.000 1 2010 2010
dbSNP: rs2197089
rs2197089 		5 0.925 0.080 8 19968862 downstream gene variant G/A snv 0.61 0.800 1.000 1 2011 2011
dbSNP: rs2206277
rs2206277
TFAP2B
4 0.925 0.080 6 50830813 intron variant C/T snv 0.19 0.800 1.000 1 2011 2011
dbSNP: rs2266788
rs2266788
ZPR1 ; APOA5
19 0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 0.800 1.000 1 2011 2011
dbSNP: rs247617
rs247617 		20 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 0.800 1.000 1 2012 2012
dbSNP: rs268
rs268
LPL
41 0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 0.800 1.000 1 2012 2012
dbSNP: rs295
rs295
LPL
1 1.000 0.040 8 19958727 intron variant A/C snv 0.28 0.800 1.000 1 2011 2011
dbSNP: rs301
rs301
LPL
7 0.925 0.160 8 19959423 intron variant T/C snv 0.24 0.26 0.800 1.000 1 2011 2011
dbSNP: rs3099844
rs3099844
MICB-DT
13 0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 0.800 1.000 1 2012 2012
dbSNP: rs3757840
rs3757840
GCK
2 1.000 0.040 7 44191617 intron variant T/C;G snv 0.800 1.000 1 2012 2012
dbSNP: rs4846922
rs4846922
GALNT2
1 1.000 0.040 1 230171436 intron variant T/A;C;G snv 0.800 1.000 1 2012 2012
dbSNP: rs496300
rs496300
LINC01679
2 1.000 0.040 21 43359800 intron variant C/T snv 0.73 0.800 1.000 1 2010 2010
dbSNP: rs569805
rs569805
ABCB11
2 1.000 0.040 2 168926370 intron variant A/T snv 0.73 0.800 1.000 1 2011 2011
dbSNP: rs6711016
rs6711016 		2 1.000 0.040 2 20923592 intergenic variant C/A snv 0.19 0.800 1.000 1 2012 2012
dbSNP: rs673548
rs673548
APOB
14 0.925 0.120 2 21014672 intron variant G/A;T snv 0.800 1.000 1 2012 2012
dbSNP: rs6947830
rs6947830 		2 0.925 0.080 7 15025359 intergenic variant G/A;C snv 0.800 1.000 1 2012 2012
dbSNP: rs782590
rs782590
PPP4R3B ; LOC107985885
1 1.000 0.040 2 55616277 intron variant C/T snv 0.44 0.800 1.000 1 2012 2012
dbSNP: rs7841189
rs7841189 		3 1.000 0.040 8 19987865 TF binding site variant C/T snv 0.15 0.800 1.000 1 2012 2012
dbSNP: rs7865146
rs7865146 		2 1.000 0.040 9 127857358 upstream gene variant C/G;T snv 0.800 1.000 1 2010 2010
dbSNP: rs8060686
rs8060686
EDC4
2 1.000 0.040 16 67877614 synonymous variant T/C snv 0.23 0.32 0.800 1.000 1 2012 2012
dbSNP: rs9939224
rs9939224
CETP
6 1.000 0.040 16 56968820 intron variant T/G snv 0.75 0.800 1.000 1 2011 2011
dbSNP: rs9940128
rs9940128
FTO
10 0.851 0.120 16 53766842 intron variant G/A snv 0.42 0.800 1.000 1 2012 2012
dbSNP: rs9987289
rs9987289
LOC157273
10 1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 0.800 1.000 1 2011 2011
dbSNP: rs2075291
rs2075291
ZPR1 ; APOA5
15 0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 0.720 1.000 3 2008 2019
dbSNP: rs651821
rs651821
APOA5
17 0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 0.720 1.000 2 2017 2017