Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 43
rs866294686
TRIM8 ; LOC105378460
0.683 0.480 10 102657073 stop gained C/A;T snv 43
rs1799963
F2
0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 25
rs121908188
SELENON
0.742 0.360 1 25809753 missense variant G/A;C snv 1.8E-04 25
rs199564797
SELENON
0.742 0.360 1 25809150 missense variant G/A snv 1.2E-05 1.4E-05 25
rs745886248
SELENON
0.742 0.360 1 25811710 missense variant G/A;C;T snv 4.3E-06; 4.3E-06; 4.3E-06 25
rs529565
ABO
0.851 0.120 9 133274084 intron variant C/T snv 13
rs9797861
SLC44A2
0.790 0.200 19 10632450 intron variant C/A;G;T snv 9
rs4444878
F11-AS1
0.851 0.120 4 186292729 intron variant C/A;T snv 7
rs7654093 0.882 0.120 4 154623920 upstream gene variant A/T snv 0.27 6
rs113092656 0.882 0.120 6 11615072 intergenic variant G/A snv 2.6E-02 5
rs60942712 0.882 0.120 3 88998609 intergenic variant G/T snv 7.9E-02 5
rs72798544
COX7A2L
0.882 0.120 2 42372465 intron variant T/G snv 1.3E-02 5
rs114209171
FUNDC2
0.882 0.120 X 155050522 non coding transcript exon variant T/C snv 0.23 5
rs34234989
MMP24-AS1-EDEM2 ; PROCR
0.882 0.120 20 35186731 intron variant A/- delins 0.40 5
rs17490626
TSPAN15
0.882 0.120 10 69458890 intron variant G/C snv 8.4E-02 5