Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs55705857
CCDC26
0.732 0.080 8 129633446 intron variant A/G snv 3.9E-02 16
rs137852578
AR
0.827 0.080 X 67723710 missense variant A/G snv 10
rs627928
RNASEL
0.790 0.080 1 182582202 missense variant A/C snv 0.54 0.49 10
rs1057519864
AR
0.851 0.080 X 67723707 missense variant T/C snv 8
rs2011077
FGFR4
0.807 0.080 5 177094455 intron variant C/T snv 0.19 8
rs976306779
AR
0.851 0.080 X 67545492 missense variant C/A;T snv 6.6E-06 8
rs11902171
ITGAV
0.925 0.080 2 186678500 3 prime UTR variant G/C snv 0.22 6
rs17650792 0.827 0.080 3 49352817 downstream gene variant A/G snv 0.42 6
rs7602358
KLHL30
0.827 0.080 2 238147187 intron variant G/T snv 0.83 6
rs119484086
ELAC2
0.851 0.080 17 12992957 missense variant C/A;T snv 4.0E-06; 5.3E-04 5
rs12653946
CTD-2194D22.4
0.882 0.080 5 1895715 intron variant C/T snv 0.43 5
rs1374051619
ELAC2
0.827 0.080 17 12995026 missense variant C/G snv 4.0E-06 5
rs137852581
AR
0.882 0.080 X 67723701 missense variant C/T snv 5
rs17632542
KLK3
0.925 0.080 19 50858501 missense variant T/C snv 5.5E-02 4.9E-02 5
rs4919743
KRT8
0.925 0.080 12 52915800 intron variant G/A snv 0.13 5
rs61552325
ERBB2
0.882 0.080 17 39727784 missense variant C/G snv 5
rs8176704
ABO
0.925 0.080 9 133260148 intron variant G/A snv 5
rs9600079 0.925 0.080 13 73154002 intergenic variant G/T snv 0.46 5
rs10175368
CYP1B1 ; CYP1B1-AS1
0.925 0.080 2 38080719 intron variant C/T snv 0.23 4
rs10505346
COLEC10 ; TNFRSF11B
0.925 0.080 8 118951604 intron variant G/T snv 0.22 4
rs1060501201
TP53
0.925 0.080 17 7674190 missense variant T/C;G snv 4
rs11102001
GSTM5 ; EPS8L3
0.925 0.080 1 109757069 missense variant G/A snv 9.4E-02 0.16 4
rs1197734477
PTEN
0.925 0.080 10 87961012 missense variant A/G snv 4
rs13083990 0.925 0.080 3 122295719 downstream gene variant T/C snv 0.30 4
rs13385191
LDAH
0.925 0.080 2 20688505 intron variant A/G snv 0.20 4