Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs3135506
APOA5
0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 17
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs2075291
APOA5 ; ZPR1
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 15
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 12