Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs2808630 0.742 0.240 1 159711078 downstream gene variant C/T snv 0.77 13
rs352162 0.882 0.160 3 52218953 non coding transcript exon variant T/C snv 0.55 3
rs1429638 0.925 0.080 4 73872213 downstream gene variant C/A;G snv 0.17 2
rs1891320 0.925 0.080 1 19970618 upstream gene variant C/T snv 0.20 2
rs653765
ADAM10
0.763 0.240 15 58749813 upstream gene variant T/C;G snv 0.45 10
rs12692386
ADAM17
0.827 0.160 2 9555777 5 prime UTR variant A/G snv 0.72 5
rs1524668
ADAM17
0.851 0.160 2 9557243 upstream gene variant A/C snv 0.64 4
rs11684747
ADAM17
0.925 0.080 2 9557042 upstream gene variant A/G snv 0.19 2
rs11689958
ADAM17
0.925 0.080 2 9557277 upstream gene variant G/A snv 0.19 2
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs17602729
AMPD1
0.925 0.080 1 114693436 stop gained G/A;T snv 8.6E-02 2
rs11216153
APOA1-AS
0.925 0.080 11 116834384 upstream gene variant G/T snv 0.16 2
rs510432
ATG5
0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 11
rs506027
ATG5
0.925 0.080 6 106326589 upstream gene variant G/A snv 0.57 2
rs4358188
BPI
0.827 0.160 20 38318446 missense variant G/A;C snv 0.46 7
rs7022797
C9orf47 ; S1PR3
0.882 0.120 9 88989548 upstream gene variant T/G snv 0.38 3
rs353291
CARMN ; MIR145
0.807 0.200 5 149431183 non coding transcript exon variant T/C snv 0.35 6
rs497116
CASP12
0.925 0.080 11 104892390 stop lost A/G snv 4.3E-02 2
rs6586282
CBS
0.882 0.080 21 43058387 intron variant C/T snv 5
rs2857656
CCL2
0.851 0.120 17 34254988 upstream gene variant G/A;C snv 5
rs2569190
CD14 ; TMCO6
0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs1129055
CD86
0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 15