Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 43
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 25
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 23
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 22
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 14
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 13
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 12
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 12
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 12
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 11
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 10
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 10
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 9
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 9
rs630014
ABO
9 133274306 intron variant G/A;C snv 9
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 9
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 8
rs12721046
APOC1
19 44917997 intron variant G/A snv 0.11 8
rs174541
FADS2
1.000 0.080 11 61798436 intron variant T/C snv 0.29 8
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 8
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 7
rs6982636 8 125467073 intron variant G/A snv 0.43 7