Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2294008
PSCA ; JRK
0.672 0.320 8 142680513 5 prime UTR variant C/T snv 0.46 0.45 28
rs2920283
JRK ; PSCA
0.925 0.040 8 142675619 intron variant T/C snv 0.44 2
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs10983755 0.790 0.320 9 117702392 upstream gene variant G/A snv 3.2E-02 7
rs10739971
MIRLET7A1 ; MIRLET7F1
0.882 0.080 9 94175398 intron variant G/A;C snv 5
rs11536878
TLR4
0.827 0.240 9 117709275 intron variant C/A snv 9.5E-02 5
rs1917799 0.851 0.120 10 49542929 upstream gene variant A/C snv 0.25 4
rs1042194
CYP2C18
1.000 0.040 10 94735727 3 prime UTR variant G/C;T snv 2
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs629367
MIR100HG ; MIRLET7A2
0.776 0.200 11 122146306 intron variant C/A snv 0.88 11
rs830083
DDB2
0.807 0.120 11 47232500 intron variant G/A;C;T snv 6
rs2029298
DDB2
0.882 0.080 11 47213167 upstream gene variant C/T snv 0.62 3
rs326222
DDB2
0.882 0.080 11 47238117 intron variant T/C snv 0.60 0.58 3
rs3781619
DDB2
0.882 0.080 11 47233766 intron variant G/A snv 0.26 3
rs2014486
MUC5B
1.000 0.040 11 1237573 intron variant A/G snv 0.52 2
rs7481521
MUC6
1.000 0.040 11 1027811 missense variant C/T snv 0.50 0.47 1
rs12229892
PTPN11
0.807 0.240 12 112485589 intron variant G/A snv 1.4E-02 6
rs2301756
PTPN11
0.851 0.120 12 112452972 intron variant A/G snv 0.21 4
rs10505799 1.000 0.040 12 16293334 intergenic variant T/C snv 0.10 2
rs12423190
PTPN11
1.000 0.040 12 112471536 intron variant T/C snv 8.7E-02 1
rs873601
BIVM-ERCC5 ; ERCC5
0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25
rs2094258
ERCC5 ; BIVM-ERCC5
0.701 0.280 13 102844409 intron variant C/T snv 0.18 20
rs9315542
LINC00571 ; LINC02334
1.000 0.040 13 38057334 intron variant T/C snv 0.26 1
rs1130233
AKT1
0.742 0.480 14 104773557 synonymous variant C/T snv 0.30 0.23 13
rs6498486
ERCC4
0.776 0.200 16 13919809 upstream gene variant A/C snv 0.27 8