Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs326118
MTRR ; FASTKD3
0.925 0.080 5 7868430 intron variant T/G snv 0.21 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
rs3019885
SLC30A8
0.925 0.120 8 117013406 intron variant T/A;G snv 2
rs3827066
ZNF335
0.925 0.040 20 45957384 intron variant C/T snv 0.12 2
rs8087799 0.882 0.080 18 22605468 regulatory region variant G/A snv 0.43 3
rs12695895
AGTR1
0.925 0.040 3 148725481 intron variant C/T snv 0.31 3
rs919433
ANKRD44 ; ANKRD44-IT1
0.882 0.080 2 197301841 intron variant G/A snv 0.38 3
rs7866503
CDKN2B-AS1
0.882 0.080 9 22091925 intron variant G/T snv 0.50 3
rs4916251
DNM3 ; PIGC
0.882 0.040 1 172377256 intron variant T/A snv 0.70 3
rs595244
FBN1
0.882 0.080 15 48548638 intron variant C/T snv 7.7E-02 3
rs12133641
IL6R
0.925 0.040 1 154455807 intron variant A/G snv 0.44 3
rs486055
MMP10 ; WTAPP1
0.925 0.120 11 102779693 missense variant C/G;T snv 1.2E-05; 0.10 3
rs8003379
MTHFD1
0.882 0.160 14 64406881 intron variant A/C snv 0.23 3
rs764522
TGFBR2 ; LOC105377015
0.882 0.080 3 30605058 upstream gene variant G/A;C snv 3
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
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
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
rs3877899
CCDC152 ; SELENOP
0.827 0.160 5 42801166 missense variant C/A;T snv 4.0E-06; 0.20 7