Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2808530
GABBR2
0.925 0.080 9 98576823 intron variant A/C snv 0.12 2
rs11689958
ADAM17
0.925 0.080 2 9557277 upstream gene variant G/A snv 0.19 2
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
rs12692386
ADAM17
0.827 0.160 2 9555777 5 prime UTR variant A/G snv 0.72 5
rs885479
MC1R
0.732 0.280 16 89919746 missense variant G/A snv 0.15 8.3E-02 16
rs11137480
S1PR3 ; C9orf47
0.882 0.120 9 88989662 upstream gene variant G/C snv 0.37 3
rs7022797
C9orf47 ; S1PR3
0.882 0.120 9 88989548 upstream gene variant T/G snv 0.38 3
rs1554162524
ELOVL4
0.882 0.160 6 79925034 splice acceptor variant T/C snv 4
rs11465996
LY96
0.790 0.240 8 73989727 upstream gene variant C/G snv 0.25 7
rs1429638 0.925 0.080 4 73872213 downstream gene variant C/A;G snv 0.17 2
rs1126647
CXCL8
0.827 0.160 4 73743328 3 prime UTR variant A/T snv 0.31 8
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1799946
DEFB1
0.732 0.360 8 6877909 5 prime UTR variant C/T snv 0.36 0.41 13
rs10506481
MIR6502 ; IRAK3
0.882 0.080 12 66250331 3 prime UTR variant T/C snv 9.0E-02 3
rs7119750
RELA
0.882 0.120 11 65655120 3 prime UTR variant C/G;T snv 3
rs842647
REL
0.827 0.400 2 60892336 intron variant G/A snv 0.62 6
rs13137
VMP1 ; MIR21
0.827 0.160 17 59841670 3 prime UTR variant A/T snv 0.18 5
rs653765
ADAM10
0.763 0.240 15 58749813 upstream gene variant T/C;G snv 0.45 10
rs1800777
CETP
0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs7096206
MBL2
0.708 0.480 10 52771925 upstream gene variant G/A;C;T snv 17
rs1800450
MBL2
0.662 0.640 10 52771475 missense variant C/T snv 0.14 0.11 26
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs352162 0.882 0.160 3 52218953 non coding transcript exon variant T/C snv 0.55 3