Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs2836411
ERG
1.000 0.040 21 38447907 intron variant C/A;T snv 1
rs5516
KLK1
0.827 0.120 19 50820217 missense variant C/G snv 0.69 0.67 6
rs1036095
TGFBR2
1.000 0.040 3 30620836 intron variant C/G snv 0.72 1
rs486055
MMP10 ; WTAPP1
0.925 0.120 11 102779693 missense variant C/G;T snv 1.2E-05; 0.10 3
rs2070863
SERPINF2
1.000 0.040 17 1745208 missense variant C/G;T snv 0.24 1
rs3918242
MMP9
0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs121917864
TLR2
0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31
rs2252070
MMP13
0.752 0.320 11 102955810 upstream gene variant C/T snv 0.68 13
rs7579
CCDC152 ; SELENOP
0.807 0.200 5 42800706 3 prime UTR variant C/T snv 0.31 0.26 6
rs12695895
AGTR1
0.925 0.040 3 148725481 intron variant C/T snv 0.31 3
rs595244
FBN1
0.882 0.080 15 48548638 intron variant C/T snv 7.7E-02 3
rs3827066
ZNF335
0.925 0.040 20 45957384 intron variant C/T snv 0.12 2
rs1057518075
MIR3606 ; COL3A1
1.000 0.040 2 188995061 stop gained C/T snv 1
rs10985349
DAB2IP
1.000 0.040 9 121662964 intron variant C/T snv 0.17 1
rs1418184396
SERPINF1
1.000 0.040 17 1776722 missense variant C/T snv 4.0E-06 1
rs1419338705
ELN
1.000 0.040 7 74048163 missense variant C/T snv 7.0E-06 1
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs5743708
TLR2
0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs1057335
SERPINF2
0.827 0.120 17 1754359 missense variant G/A snv 0.22 0.20 5