Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs764522
TGFBR2 ; LOC105377015
0.882 0.080 3 30605058 upstream gene variant G/A;C snv 3
rs7866503
CDKN2B-AS1
0.882 0.080 9 22091925 intron variant G/T snv 0.50 3
rs8003379
MTHFD1
0.882 0.160 14 64406881 intron variant A/C snv 0.23 3
rs8087799 0.882 0.080 18 22605468 regulatory region variant G/A snv 0.43 3
rs919433
ANKRD44 ; ANKRD44-IT1
0.882 0.080 2 197301841 intron variant G/A snv 0.38 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
rs3019885
SLC30A8
0.925 0.120 8 117013406 intron variant T/A;G snv 2
rs326118
MTRR ; FASTKD3
0.925 0.080 5 7868430 intron variant T/G snv 0.21 2
rs3827066
ZNF335
0.925 0.040 20 45957384 intron variant C/T snv 0.12 2
rs4988300
LRP5
0.925 0.120 11 68321363 intron variant G/T snv 0.50 2
rs773474756
MMP1 ; WTAPP1
0.925 0.080 11 102790467 missense variant T/C snv 8.1E-06 2
rs1036095
TGFBR2
1.000 0.040 3 30620836 intron variant C/G snv 0.72 1
rs1057518075
MIR3606 ; COL3A1
1.000 0.040 2 188995061 stop gained C/T snv 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
rs13382862
LDAH
1.000 0.040 2 20682689 upstream gene variant A/G;T snv 0.59 1
rs1385526
LRP1
1.000 0.040 12 57138966 intron variant G/C snv 0.26 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
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
rs2306691
LRP1-AS ; LRP1
1.000 0.040 12 57145019 missense variant A/G snv 2.0E-05 2.1E-05 1