Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519912
MED12
0.776 0.200 X 71129408 missense variant C/G;T snv 5
rs137852564
AR
0.827 0.240 X 67722976 missense variant G/A;T snv 5
rs1327301 0.882 0.160 X 51467205 downstream gene variant C/T snv 0.29 3
rs137852569
AR
0.752 0.320 X 67686030 missense variant G/A snv 9.4E-06 3
rs137852591
AR
0.851 0.200 X 67721909 missense variant C/G snv 1.4E-03 1.4E-03 3
rs5919432 0.882 0.160 X 67801708 intergenic variant C/T snv 3
rs5945572 0.882 0.160 X 51486831 downstream gene variant A/G snv 3
rs5945619
LINC01496
0.882 0.160 X 51498820 non coding transcript exon variant C/T snv 3
rs137852567
AR
0.882 0.200 X 67717595 missense variant A/G snv 2
rs137852571
AR
0.882 0.080 X 67717495 missense variant G/A snv 7.7E-05 1.9E-05 2
rs137852578
AR
0.827 0.080 X 67723710 missense variant A/G snv 2
rs137852580
AR
0.925 0.080 X 67723711 missense variant C/G;T snv 2
rs137852581
AR
0.882 0.080 X 67723701 missense variant C/T snv 2
rs137852582
AR
0.925 0.080 X 67723786 missense variant A/G snv 2
rs137852583
AR
0.925 0.080 X 67711680 missense variant G/A snv 2
rs137852584
AR
0.925 0.080 X 67711459 missense variant G/A snv 2
rs137852593
AR
0.827 0.160 X 67717484 missense variant G/A;C;T snv 2.2E-05; 1.1E-05; 9.1E-04 2
rs2405942
SHROOM2
0.925 0.080 X 9846095 intron variant G/A snv 2
rs864622007
AR
0.882 0.200 X 67711621 missense variant T/A snv 2
rs1340026226
AR
1.000 0.080 X 67711662 missense variant G/A snv 9.5E-06 1
rs138454018
AR
1.000 0.080 X 67546171 missense variant C/A;T snv 4.4E-05; 4.9E-05 1
rs1419040 1.000 0.080 X 51609183 intergenic variant G/A snv 1
rs4604628 1.000 0.080 X 51644318 intergenic variant C/G;T snv 1
rs5991735
MAGED1
1.000 0.080 X 51809788 intron variant G/A;C snv 1
rs6624304
AR
0.882 0.160 X 67655914 intron variant T/A;C snv 1