Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1036095
TGFBR2
1.000 0.040 3 30620836 intron variant C/G snv 0.72 1
rs10758278
PHF24
1.000 0.040 9 34825306 intron variant G/A snv 0.53 1
rs10985349
DAB2IP
1.000 0.040 9 121662964 intron variant C/T snv 0.17 1
rs1385526
LRP1
1.000 0.040 12 57138966 intron variant G/C snv 0.26 1
rs2652106
VCAN
1.000 0.040 5 83498217 intron variant G/T snv 0.39 1
rs2836411
ERG
1.000 0.040 21 38447907 intron variant C/A;T snv 1
rs3781590
LRP5
1.000 0.040 11 68391684 intron variant G/A snv 0.35 1
rs58749629
PCIF1
1.000 0.040 20 45942678 intron variant G/A;T snv 0.13 1
rs6674171
TDRD10
1.000 0.040 1 154519207 intron variant A/G;T snv 0.19 1
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs1795061 1.000 0.040 1 214235937 intergenic variant T/C;G snv 1
rs9316871 1.000 0.040 13 22287782 intergenic variant A/G snv 0.22 1
rs8087799 0.882 0.080 18 22605468 regulatory region variant G/A snv 0.43 3
rs1057518075
MIR3606 ; COL3A1
1.000 0.040 2 188995061 stop gained C/T snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
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
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
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
rs121917864
TLR2
0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31
rs2043211
CARD8
0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29