Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1491850 0.925 0.080 11 27728178 intron variant T/C snv 0.37 1
rs7713917 0.925 0.040 5 79533426 upstream gene variant A/G snv 0.54 1
rs8007267 0.882 0.200 14 54912273 intergenic variant C/T snv 0.31 1
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 1
rs841
GCH1
0.827 0.200 14 54843774 splice region variant G/A snv 0.22 0.22 1
rs11123857
NPAS2
2 100987350 non coding transcript exon variant A/G snv 0.29 1
rs2522833
PCLO
0.827 0.080 7 82824392 missense variant A/C snv 0.45 0.34 1
rs717454
REV1
1.000 0.040 2 99406310 non coding transcript exon variant T/C;G snv 0.44; 8.2E-06 1
rs659366
UCP2
0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 1
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 1
rs10020288 1.000 0.040 4 28686220 intergenic variant G/A snv 0.38 2
rs10156548 1.000 0.040 9 23318435 intron variant G/C;T snv 2
rs10429537 1.000 0.040 9 23346844 intron variant C/G snv 0.33 2
rs10891564 1.000 0.040 11 113503291 intergenic variant G/A snv 0.34 2
rs11826064 1.000 0.040 11 50818695 intergenic variant C/A;T snv 2
rs12030991 1.000 0.040 1 106683737 intergenic variant G/C;T snv 2
rs12420205 1.000 0.040 11 113523313 intergenic variant C/T snv 0.65 2
rs13296664 1.000 0.040 9 117684418 downstream gene variant C/T snv 0.22 2
rs1360380 1.000 0.040 9 23378490 intron variant G/A;T snv 2
rs1427027 1.000 0.040 18 37666359 intron variant C/G;T snv 2
rs145097508 1.000 0.040 6 28714629 intergenic variant G/C snv 3.1E-02 2
rs17570807 1.000 0.040 18 37662673 intron variant A/G snv 3.1E-02 2
rs1782179 1.000 0.040 14 41224737 intergenic variant T/A;C snv 2
rs182087934 2 183742707 intergenic variant G/A snv 2
rs190544851 1.000 0.040 21 38360474 intergenic variant T/G snv 4.8E-03 2