Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs99780
FADS1 ; FADS2
1.000 0.080 11 61829161 intron variant C/T snv 0.38 3
rs996876302
PECAM1
17 64363155 missense variant C/T snv 3.5E-05 1
rs995922697
GPX1
0.724 0.560 3 49357413 missense variant A/G snv 4.1E-06 15
rs9944411
FBXL20
17 39327346 intron variant T/C snv 0.32 2
rs9895661
BCAS3
0.882 0.200 17 61379228 non coding transcript exon variant C/T snv 0.69 10
rs9846911 3 187500548 intergenic variant A/G snv 0.47 2
rs9749262
CERS4
1.000 0.080 19 8223873 intron variant C/A;G;T snv 2
rs97384
FADS2
1.000 0.080 11 61856709 non coding transcript exon variant T/C snv 0.46 5
rs968567
FADS2 ; FADS1
0.851 0.240 11 61828092 intron variant C/T snv 0.11 7
rs9658625
SOAT2
12 53103618 missense variant A/G snv 9.3E-02 7.4E-02 1
rs953038635
SOD2
0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs9319428
FLT1
0.925 0.080 13 28399484 intron variant G/A snv 0.30 4
rs911119
CST3
0.807 0.120 20 23632100 non coding transcript exon variant C/G;T snv 9
rs883484 9 122362748 intergenic variant C/T snv 0.20 1
rs881858
LOC105375069 ; LOC107986598
0.882 0.200 6 43838872 intron variant G/A;C snv 7
rs850799 1.000 0.080 15 23679185 intergenic variant T/G snv 0.20 2
rs814698
ZNF618
1.000 0.080 9 113967563 intron variant A/T snv 0.22 2
rs8101881 19 32873722 upstream gene variant C/T snv 0.54 2
rs8008070
SYNE2
1.000 0.080 14 63767002 intron variant A/T snv 0.23 2
rs79741405 1.000 0.080 6 160673237 intron variant G/T snv 9.9E-02 2
rs7943728
MYRF ; TMEM258
1.000 0.080 11 61779596 intron variant G/A snv 0.12 0.11 3
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs7901695
TCF7L2
0.851 0.160 10 112994329 intron variant T/C snv 0.34 6
rs78351985
C4orf54
4 99655532 upstream gene variant A/G snv 3.2E-04 1
rs7805747
PRKAG2
1.000 0.080 7 151710715 intron variant G/A snv 0.26 5