Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs763059810
CXCR4
0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs1265538677
CPB2-AS1 ; CPB2
0.790 0.200 13 46055808 synonymous variant A/G snv 4.0E-06 10
rs1417938
CRP
0.776 0.320 1 159714396 intron variant T/A;C snv 0.28 10
rs1466535
LRP1
0.790 0.160 12 57140687 intron variant G/A;C snv 9
rs3877899
CCDC152 ; SELENOP
0.827 0.160 5 42801166 missense variant C/A;T snv 4.0E-06; 0.20 7
rs12191786
CASC15
0.851 0.120 6 22004398 intron variant C/A;T snv 4
rs61758388
LOC107987234 ; XYLT1
0.851 0.360 16 17470454 missense variant C/A;G snv 2.7E-02 4
rs486055
MMP10 ; WTAPP1
0.925 0.120 11 102779693 missense variant C/G;T snv 1.2E-05; 0.10 3
rs764522
TGFBR2 ; LOC105377015
0.882 0.080 3 30605058 upstream gene variant G/A;C snv 3
rs137854485
FBN1
0.925 0.160 15 48515402 missense variant G/A snv 2
rs201191171
SLC12A5-AS1 ; MMP9
0.925 0.080 20 46013279 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 2
rs2234681
MMP9
1.000 0.040 20 46008773 upstream gene variant ACACACACACACACACACACACAC/-;AC;ACAC;ACACAC;ACACACAC;ACACACACAC;ACACACACACAC;ACACACACACACAC;ACACACACACACACAC;ACACACACACACACACAC;ACACACACACACACACACAC;ACACACACACACACACACACAC;ACACACACACACACACACACACACAC;ACACACACACACACACACACACACACAC;ACACACACACACACACACACACACACACAC;ACACACACACACACACACACACACACACACAC;ACACACACACACACACACACACACACACACACAC delins 2
rs3019885
SLC30A8
0.925 0.120 8 117013406 intron variant T/A;G snv 2
rs773474756
MMP1 ; WTAPP1
0.925 0.080 11 102790467 missense variant T/C snv 8.1E-06 2
rs1057518075
MIR3606 ; COL3A1
1.000 0.040 2 188995061 stop gained C/T snv 1
rs1418184396
SERPINF1
1.000 0.040 17 1776722 missense variant C/T snv 4.0E-06 1
rs1795061 1.000 0.040 1 214235937 intergenic variant T/C;G snv 1
rs2070863
SERPINF2
1.000 0.040 17 1745208 missense variant C/G;T snv 0.24 1