Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs186696265 0.882 0.040 6 160690668 intergenic variant C/T snv 1.0E-02 6
rs2075252
LRP2
0.925 0.160 2 169154475 stop gained T/A;C snv 0.76 5
rs4668123
LRP2
0.851 0.280 2 169196995 missense variant C/A;G;T snv 6
rs5361
SELE ; C1orf112
0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs12696304 0.776 0.320 3 169763483 downstream gene variant C/G snv 0.38 10
rs12766939
CUBN
0.925 0.160 10 17031136 intron variant A/G snv 0.23 2
rs1801222
CUBN
0.925 0.160 10 17114152 missense variant A/G snv 0.73 0.72 5
rs201052613 0.882 0.080 1 173026503 intron variant T/-;TT delins 9.4E-03 3
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14 17
rs1234314
TNFSF4
0.790 0.320 1 173208253 upstream gene variant C/A;G snv 7
rs8075977 0.827 0.160 17 1757507 upstream gene variant T/C snv 0.37 5
rs5940
LOC105373786 ; TFPI
0.882 0.080 2 187466977 missense variant C/T snv 1.3E-02 1.4E-02 3
rs11573156
PLA2G2A
0.882 0.240 1 19979653 5 prime UTR variant G/C snv 0.19 5
rs747112750
LGR6
1.000 0.040 1 202307363 synonymous variant C/T snv 4.0E-06 1
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24
rs113681054 1.000 0.040 12 21250045 intergenic variant T/C snv 0.18 1
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs10811656
CDKN2B-AS1
0.807 0.200 9 22124473 intron variant C/T snv 0.47 7
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs1333047
CDKN2B-AS1
0.790 0.240 9 22124505 intron variant A/T snv 0.63 9
rs10757279
CDKN2B-AS1
0.925 0.040 9 22124631 intron variant A/G snv 0.40 3
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60