Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs4898
TIMP1 ; SYN1 ; MIR4769
0.672 0.520 X 47585586 synonymous variant T/C snv 0.46 0.46 25
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs2276109
MMP12
0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 18
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
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs2252070
MMP13
0.752 0.320 11 102955810 upstream gene variant C/T snv 0.68 13
rs12916
HMGCR ; CERT1
0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37 12
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 10
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
rs2070584
TIMP1 ; MIR4769 ; SYN1
0.790 0.200 X 47587120 intron variant T/G snv 0.44 8
rs3877899
CCDC152 ; SELENOP
0.827 0.160 5 42801166 missense variant C/A;T snv 4.0E-06; 0.20 7
rs7579
CCDC152 ; SELENOP
0.807 0.200 5 42800706 3 prime UTR variant C/T snv 0.31 0.26 6
rs5516
KLK1
0.827 0.120 19 50820217 missense variant C/G snv 0.69 0.67 6
rs12692386
ADAM17
0.827 0.160 2 9555777 5 prime UTR variant A/G snv 0.72 5
rs1057335
SERPINF2
0.827 0.120 17 1754359 missense variant G/A snv 0.22 0.20 5
rs1524668
ADAM17
0.851 0.160 2 9557243 upstream gene variant A/C snv 0.64 4
rs12191786
CASC15
0.851 0.120 6 22004398 intron variant C/A;T snv 4
rs7025486
DAB2IP
0.851 0.040 9 121660124 intron variant G/A snv 0.28 4
rs61758388
LOC107987234 ; XYLT1
0.851 0.360 16 17470454 missense variant C/A;G snv 2.7E-02 4
rs2479409
PCSK9
1.000 0.040 1 55038977 upstream gene variant G/A snv 0.66 4