Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs1057519912
MED12
0.776 0.200 X 71129408 missense variant C/G;T snv 11
rs137852569
AR
0.752 0.320 X 67686030 missense variant G/A snv 9.4E-06 10
rs137852578
AR
0.827 0.080 X 67723710 missense variant A/G snv 10
rs6152
AR
0.763 0.240 X 67545785 synonymous variant G/A snv 0.15 0.28 9
rs1057519864
AR
0.851 0.080 X 67723707 missense variant T/C snv 8
rs137852593
AR
0.827 0.160 X 67717484 missense variant G/A;C;T snv 2.2E-05; 1.1E-05; 9.1E-04 8
rs976306779
AR
0.851 0.080 X 67545492 missense variant C/A;T snv 6.6E-06 8
rs137852581
AR
0.882 0.080 X 67723701 missense variant C/T snv 5
rs864622007
AR
0.882 0.200 X 67711621 missense variant T/A snv 5
rs1034866440
AR
0.851 0.160 X 67643401 missense variant G/A snv 5.7E-06 4
rs1327301 0.882 0.160 X 51467205 downstream gene variant C/T snv 0.29 3
rs137852571
AR
0.882 0.080 X 67717495 missense variant G/A snv 7.7E-05 1.9E-05 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
rs6624304
AR
0.882 0.160 X 67655914 intron variant T/A;C snv 3
rs968098233
AR
0.882 0.200 X 67546162 missense variant T/C snv 3
rs139756052
AR
0.925 0.080 X 67643314 missense variant A/T snv 1.3E-04 5.6E-04 2
rs17302090 0.925 0.080 X 67535561 downstream gene variant G/A snv 8.5E-02 2
rs2315123
OPN1LW
0.925 0.080 X 154156372 missense variant T/C;G snv 5.5E-06 2
rs2405942
SHROOM2
0.925 0.080 X 9846095 intron variant G/A snv 2
rs5945372
PNMA6E ; LOC105373379
0.925 0.080 X 153400456 intron variant A/C;T snv 2
rs7064929
ZC3H12B
0.925 0.120 X 65147139 intergenic variant G/A snv 0.25 2
rs75759941
RPGR
0.925 0.080 X 38291789 intron variant T/C snv 7.5E-02 2