Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2241220
ACACB
1.000 0.040 12 109237224 synonymous variant T/A;C;G snv 4.0E-06; 0.83 2
rs4072032
PECAM1
1.000 0.040 17 64378896 intron variant G/A snv 0.40 2
rs41284589
SPATA1 ; GNG5
1.000 0.040 1 84506243 5 prime UTR variant G/A snv 5.4E-02 2
rs4646234
SLC15A1
1.000 0.040 13 98684126 3 prime UTR variant T/C snv 0.11 2
rs574363219
APOA5 ; ZPR1
1.000 0.040 11 116790427 missense variant C/T snv 1.4E-04 2
rs6066394
NCOA3
1.000 0.040 20 47581409 intron variant C/T snv 0.29 2
rs957970
STAT3
1.000 0.040 17 42367872 intron variant A/G snv 0.36 2
rs4845625
IL6R
0.851 0.080 1 154449591 intron variant T/C snv 0.60 9
rs5128
APOC3
0.925 0.080 11 116832924 3 prime UTR variant G/C snv 0.84 0.87 8
rs6982502 0.882 0.080 8 125467120 intron variant C/T snv 0.62 6
rs121918394
APOE
0.882 0.080 19 44908786 missense variant A/C;G snv 6.5E-06 5
rs2569512
ILF3
0.925 0.080 19 10679486 intron variant T/C snv 0.76 5
rs11635252
CRTC3
0.925 0.080 15 90528542 upstream gene variant T/C snv 0.88 4
rs201079485
ZPR1 ; APOA5
0.925 0.080 11 116790940 stop gained G/A;T snv 8.0E-05; 4.0E-06 4
rs587777636
GPIHBP1
0.882 0.080 8 143213935 missense variant G/A;C snv 6.5E-06 4
rs121909397
LMF1
0.925 0.080 16 869982 stop gained G/A;C snv 1.6E-04; 4.0E-06 3
rs190853081
APOE
0.925 0.080 19 44909083 missense variant G/A snv 2.0E-04 5.6E-05 3
rs2187331
LOC107984343
0.925 0.080 11 68678956 upstream gene variant C/T snv 0.84 3
rs3862434
CRTC3
1.000 0.080 15 90537155 intron variant A/G snv 0.48 3
rs774006043
ZPR1 ; APOA5
0.925 0.080 11 116790561 missense variant C/T snv 3
rs972283
LOC105375508
1.000 0.080 7 130782095 intergenic variant A/G;T snv 3
rs11634397 1.000 0.080 15 80139880 downstream gene variant A/G snv 0.57 2
rs1378577
ABCG1
1.000 0.080 21 42199555 upstream gene variant T/G snv 0.33 2
rs2808607
EGLN1
1.000 0.080 1 231405228 intron variant G/A snv 0.56 2
rs35414700
LPL
1.000 0.080 8 19955901 missense variant T/G snv 1.2E-05 1.4E-05 2