Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35414700
LPL
1.000 0.080 8 19955901 missense variant T/G snv 1.2E-05 1.4E-05 1
rs770601263
LPL
1.000 0.080 8 19954273 missense variant T/G snv 8.0E-06 1
rs886037774
LPL
0.882 0.120 8 19955993 missense variant T/C snv 6
rs1161884343
LPL
1.000 0.080 8 19955930 missense variant T/C snv 7.0E-06 1
rs1181582051
LPL
1.000 0.080 8 19956048 missense variant T/C snv 4.0E-06 1
rs118204061
LPL
1.000 0.080 8 19954240 missense variant T/C snv 1.6E-05 4.2E-05 1
rs118204069
LPL
1.000 0.080 8 19951856 missense variant T/C snv 7.0E-06 1
rs118204080
LPL
1.000 0.080 8 19954333 missense variant T/C snv 2.0E-05 1
rs773235712
LPL
1.000 0.080 8 19955978 missense variant T/C snv 4.0E-06 1
rs528243561
LPL
1.000 0.080 8 19954258 missense variant T/A;C snv 3.6E-05 1
rs118204059
LPL
1.000 0.080 8 19955876 missense variant T/A snv 1
rs118204065
LPL
1.000 0.080 8 19951783 stop gained T/A snv 4.0E-06 1
rs766134215
LPL
1.000 0.080 8 19939529 splice donor variant G/C;T snv 8.7E-06; 4.4E-06; 4.4E-06 1
rs373088068
LPL
1.000 0.080 8 19951805 missense variant G/C snv 9.9E-05 1.3E-04 1
rs748349562
LPL
1.000 0.080 8 19954131 missense variant G/A;T snv 4.0E-06; 4.0E-06 1
rs118204057
LPL
0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 2
rs1800011
LPL
1.000 0.080 8 19955927 missense variant G/A;C snv 6.0E-05 1
rs1801177
LPL
0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 1
rs781614031
LPL
1.000 0.080 8 19954125 missense variant G/A;C snv 4.0E-06 1
rs118204056
LPL
1.000 0.080 8 19954185 missense variant G/A snv 7.0E-06 1
rs118204062
LPL
1.000 0.080 8 19955874 missense variant G/A snv 4.0E-06 1.4E-05 1
rs118204063
LPL
1.000 0.080 8 19953386 missense variant G/A snv 4.0E-06 1
rs118204066
LPL
1.000 0.080 8 19960988 stop gained G/A snv 1
rs118204068
LPL
0.925 0.120 8 19955894 missense variant G/A snv 1.6E-05 1.4E-05 1
rs118204070
LPL
1.000 0.080 8 19951791 stop gained G/A snv 4.0E-06 3.5E-05 1