Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 14
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 13
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 13
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 12
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 12
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 12
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 11
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 11
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 11
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 11
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 10
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 10
rs445925
APOC1
0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 10
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 10
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 10
rs2228671
LDLR
0.790 0.160 19 11100236 stop gained C/A;G;T snv 1.6E-05; 8.9E-02 10
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 10
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 10
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 9
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 9
rs630014
ABO
9 133274306 intron variant G/A;C snv 9
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 9
rs5742904
APOB
0.689 0.280 2 21006288 missense variant C/A;T snv 2.8E-04 7.3E-04 9
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 9
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 9