Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1878406 0.807 0.200 4 147472512 intergenic variant C/A;G;T snv 7
rs3861950
TNFSF4
0.827 0.160 1 173187153 intron variant T/C snv 0.47 7
rs4380028
MORF4L1
0.807 0.120 15 78818751 intron variant C/T snv 0.34 7
rs4773144
COL4A1 ; COL4A2
0.827 0.080 13 110308365 intron variant A/G snv 0.42 7
rs587745372
GJA5 ; LOC102723321
0.851 0.240 1 147773383 upstream gene variant T/A snv 2.8E-05 7
rs879254693
LDLR
0.807 0.160 19 11107424 missense variant T/A;C;G snv 7
rs1008438
HSPA1L ; HSPA1A
0.807 0.120 6 31815431 upstream gene variant A/C;T snv 6
rs2453021
TNFRSF9
0.807 0.080 1 7929506 intron variant C/A;T snv 6
rs2943650 0.827 0.120 2 226241205 intergenic variant C/T snv 0.58 6
rs353291
CARMN ; MIR145
0.807 0.200 5 149431183 non coding transcript exon variant T/C snv 0.35 6
rs6495446
MTHFS ; ST20-MTHFS
0.851 0.200 15 79862640 intron variant C/T snv 0.31 6
rs7439293
PALLD
0.807 0.080 4 168756335 non coding transcript exon variant G/A snv 0.44 6
rs759003763
MIR6886 ; LDLR
0.827 0.120 19 11113585 missense variant G/A snv 6
rs974819 0.807 0.080 11 103789839 intron variant T/A;C snv 6
rs12564445
TNNT2
0.851 0.040 1 201376359 intron variant G/A snv 0.27 5
rs1384889210
APOA1 ; APOA1-AS
0.827 0.040 11 116836193 missense variant C/A snv 5
rs213045
ECE1
0.851 0.120 1 21290752 intron variant G/T snv 0.44 5
rs2144908
LOC105372629 ; HNF4A
0.851 0.120 20 44357077 intron variant G/A snv 0.18 5
rs2820315
LMOD1
0.882 0.040 1 201903136 intron variant C/T snv 0.23 5
rs4076317
ANGPTL4
0.882 0.080 19 8364115 intron variant C/G snv 0.25 5
rs7217186
ALOX15
0.827 0.120 17 4636097 intron variant C/T snv 0.45 5
rs879254840
LDLR ; MIR6886
0.827 0.120 19 11113322 missense variant A/G snv 5
rs9289231
KALRN
0.827 0.120 3 124055231 intergenic variant T/G snv 0.15 5
rs12762303
ALOX5
0.851 0.080 10 45373723 upstream gene variant T/C snv 0.17 4
rs1298417395
COP1
0.882 0.080 1 176206716 missense variant C/T snv 1.4E-05 4