Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs320
LPL
0.827 0.200 8 19961566 intron variant T/A;G snv 3
rs325
LPL
8 19961817 intron variant T/C snv 9.0E-02 4
rs326
LPL
8 19961928 intron variant A/G snv 0.37 3
rs327
LPL
8 19962025 intron variant T/G snv 0.31 4
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 7
rs331
LPL
8 19962894 intron variant G/A snv 0.30 3
rs12679834
LPL
8 19962922 intron variant T/C snv 9.4E-02 5
rs10099160
LPL
8 19964304 intron variant T/G snv 0.20 2
rs4922115
LPL
8 19965319 3 prime UTR variant G/A snv 0.15 0.14 3
rs3289
LPL
8 19965681 3 prime UTR variant T/C snv 4.0E-02 3
rs11570892
LPL
8 19966106 3 prime UTR variant A/G;T snv 3
rs3208305
LPL
1.000 0.080 8 19966137 3 prime UTR variant A/T snv 0.36 3
rs1059507
LPL
1.000 0.080 8 19966452 3 prime UTR variant C/T snv 0.15 3
rs3735964
LPL
1.000 0.080 8 19966534 3 prime UTR variant C/A snv 9.1E-02 4
rs3200218
LPL
8 19966560 3 prime UTR variant A/G;T snv 3
rs13702
LPL
0.925 0.160 8 19966981 3 prime UTR variant T/A;C snv 3
rs15285
LPL
1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36 1
rs3916027
LPL
8 19967357 downstream gene variant G/A snv 0.31 3
rs9644636
LPL
8 19967385 downstream gene variant T/A;G snv 3
rs4921683
LPL
8 19967557 downstream gene variant T/A snv 0.14 3