Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs11591147
PCSK9
0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 22
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 17
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs2228671
LDLR
0.790 0.160 19 11100236 stop gained C/A;G;T snv 1.6E-05; 8.9E-02 14
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 12
rs2228603
NCAN
0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 12
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 12
rs1042031
APOB
0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 11
rs4148217
ABCG8
0.790 0.280 2 43872294 missense variant C/A;T snv 0.21; 1.2E-05 11
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 11
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 10
rs445925
APOC1
0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 10
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 10
rs630014
ABO
9 133274306 intron variant G/A;C snv 9
rs4245791
ABCG8
0.882 0.080 2 43847292 non coding transcript exon variant C/A;T snv 8
rs11570255
EDN3
1.000 20 59300861 missense variant G/A;T snv 3.3E-03; 2.9E-05 7
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 7
rs11571151
PGR-AS1 ; PGR
11 101127486 missense variant C/G;T snv 6