Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7069102
SIRT1
0.790 0.440 10 67903362 intron variant C/G snv 0.64 10
rs9895661
BCAS3
0.882 0.200 17 61379228 non coding transcript exon variant C/T snv 0.69 10
rs3816527
PTX3 ; VEPH1
0.882 0.160 3 157437525 missense variant C/A snv 0.64 0.64 9
rs4362
ACE
0.807 0.240 17 63496400 missense variant T/C;G snv 0.52; 1.2E-05 0.51 9
rs4821480
MYH9
0.807 0.160 22 36299201 intron variant G/T snv 0.78 9
rs4845625
IL6R
0.851 0.080 1 154449591 intron variant T/C snv 0.60 9
rs7754840
CDKAL1
0.807 0.200 6 20661019 intron variant G/A;C;T snv 9
rs911119
CST3
0.807 0.120 20 23632100 non coding transcript exon variant C/G;T snv 9
rs1126616
SPP1
0.827 0.280 4 87982701 synonymous variant C/G;T snv 0.32 0.26 8
rs1367117
APOB
1.000 0.080 2 21041028 missense variant G/A snv 0.26 0.24 8
rs174541
FADS2
1.000 0.080 11 61798436 intron variant T/C snv 0.29 8
rs174566
FADS1 ; FADS2
0.925 0.160 11 61824890 intron variant A/G snv 0.34 8
rs2296545
LIPJ ; RNLS
0.851 0.160 10 88583080 missense variant C/G;T snv 0.46 8
rs4293393
UMOD
0.827 0.200 16 20353266 intron variant A/G snv 0.20 8
rs46522
UBE2Z
0.807 0.120 17 48911235 non coding transcript exon variant C/T snv 0.40 8
rs1171614
SLC16A9
0.882 0.200 10 59709780 5 prime UTR variant T/C snv 0.79 7
rs11864909
PDILT
0.851 0.160 16 20389517 intron variant C/T snv 0.23 7
rs1394125
UBE2Q2
0.882 0.200 15 75866642 intron variant G/A;T snv 7
rs174554
FADS1 ; FADS2
1.000 0.080 11 61811991 intron variant A/G snv 0.40 0.28 7
rs174574
FADS2
1.000 0.080 11 61832870 intron variant A/C snv 0.55 7
rs267734 0.925 0.120 1 150979001 upstream gene variant T/C snv 0.14 7
rs3752462
MYH9
0.827 0.160 22 36314138 splice region variant T/C snv 0.57 0.53 7
rs3925584
LOC101928338
1.000 0.080 11 30738788 intergenic variant T/C snv 0.35 7
rs4014195 0.882 0.200 11 65739351 intergenic variant C/G snv 0.31 7
rs4773144
COL4A1 ; COL4A2
0.827 0.080 13 110308365 intron variant A/G snv 0.42 7