Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7866503
CDKN2B-AS1
0.882 0.080 9 22091925 intron variant G/T snv 0.50 3
rs1265538677
CPB2-AS1 ; CPB2
0.790 0.200 13 46055808 synonymous variant A/G snv 4.0E-06 10
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs1417938
CRP
0.776 0.320 1 159714396 intron variant T/A;C snv 0.28 10
rs763059810
CXCR4
0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs7025486
DAB2IP
0.851 0.040 9 121660124 intron variant G/A snv 0.28 4
rs10985349
DAB2IP
1.000 0.040 9 121662964 intron variant C/T snv 0.17 1
rs4916251
DNM3 ; PIGC
0.882 0.040 1 172377256 intron variant T/A snv 0.70 3
rs1419338705
ELN
1.000 0.040 7 74048163 missense variant C/T snv 7.0E-06 1
rs782591769
ELN
1.000 0.040 7 74045237 missense variant G/C snv 8.0E-06 1
rs2836411
ERG
1.000 0.040 21 38447907 intron variant C/A;T snv 1
rs595244
FBN1
0.882 0.080 15 48548638 intron variant C/T snv 7.7E-02 3
rs137854485
FBN1
0.925 0.160 15 48515402 missense variant G/A snv 2
rs12916
HMGCR ; CERT1
0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37 12
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs12133641
IL6R
0.925 0.040 1 154455807 intron variant A/G snv 0.44 3
rs5516
KLK1
0.827 0.120 19 50820217 missense variant C/G snv 0.69 0.67 6
rs13382862
LDAH
1.000 0.040 2 20682689 upstream gene variant A/G;T snv 0.59 1
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs61758388
LOC107987234 ; XYLT1
0.851 0.360 16 17470454 missense variant C/A;G snv 2.7E-02 4
rs1466535
LRP1
0.790 0.160 12 57140687 intron variant G/A;C snv 9