Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs737582
CNTN5
1.000 0.040 11 99992669 intron variant G/A snv 0.39 1
rs7678287
SLC2A9 ; LOC105374476
1.000 0.080 4 9998877 intron variant A/C;G;T snv 1
rs7754794
MCHR2
1.000 0.040 6 99984779 intron variant C/A;T snv 1
rs1831992
ZIC2
1.000 0.080 13 99983123 synonymous variant C/T snv 8.1E-02 7.8E-02 2
rs6590474
CNTN5
1.000 0.040 11 99982441 intron variant A/C snv 0.71 1
rs4215
AZGP1
1.000 0.080 7 99971771 missense variant G/A;C snv 0.41 1
rs2276939
H2AZ1-DT ; H2AZ1
1.000 0.040 4 99949218 non coding transcript exon variant T/A;G snv 1
rs10014424
DNAJB14
1.000 0.040 4 99943207 intron variant G/A snv 6.2E-02 1
rs6854536
DNAJB14
1.000 0.040 4 99941725 intron variant T/A;C snv 1
rs3775948
LOC105374476 ; SLC2A9
0.882 0.160 4 9993558 intron variant G/A;C snv 1
rs11974610
GJC3
7 99930354 intron variant G/A snv 0.30 2
rs6449213
SLC2A9 ; LOC105374476
0.827 0.240 4 9992591 intron variant C/T snv 0.82 3
rs118203964
AGL
0.882 0.080 1 99916492 missense variant G/C snv 2
rs267606640
AGL
0.882 0.120 1 99913557 stop gained G/A snv 5.6E-05 5.6E-05 4
rs113994131
AGL
0.925 0.080 1 99902776 stop gained C/A;T snv 4.0E-06; 8.0E-06 1
rs267606639
AGL
0.925 0.080 1 99900712 missense variant A/G snv 1
rs3740058
DNMBP
1.000 0.080 10 99896225 intron variant G/A snv 0.34 0.31 1
rs2298735
LAMTOR3
4 99894460 upstream gene variant A/C snv 0.44 1
rs76665876
TRIM4
7 99892234 missense variant G/A snv 4.5E-03 1.3E-03 1
rs148972953
LAMTOR3
0.925 0.080 4 99881589 3 prime UTR variant A/G snv 8.8E-03 3
rs11190305
DNMBP
1.000 0.080 10 99880120 missense variant A/C;G snv 0.34; 8.0E-06 1
rs11944405
LAMTOR3
0.925 0.080 4 99878804 3 prime UTR variant T/C snv 0.28 2
rs11190302 1.000 0.080 10 99873158 downstream gene variant C/T snv 0.37 1
rs755747010
AGL
1.000 0.080 1 99870764 stop gained C/T snv 8.0E-06 7.0E-06 1
rs1131339
STX17-AS1 ; NR4A3
0.925 0.080 9 99865020 3 prime UTR variant A/G snv 0.45 2