Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs28934578
TP53
0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs6259
SHBG
0.658 0.400 17 7633209 missense variant G/A snv 8.9E-02 8.1E-02 27
rs523349
SRD5A2
0.689 0.440 2 31580636 missense variant G/A;C;T snv 0.66; 4.9E-06 21
rs10993994
MSMB
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54 15
rs627928
RNASEL
0.790 0.080 1 182582202 missense variant A/C snv 0.54 0.49 10
rs4242382 0.763 0.240 8 127505328 intergenic variant A/G;T snv 9
rs976306779
AR
0.851 0.080 X 67545492 missense variant C/A;T snv 6.6E-06 8
rs2011077
FGFR4
0.807 0.080 5 177094455 intron variant C/T snv 0.19 8
rs41341748
MSR1
0.827 0.120 8 16155085 stop gained G/A;C snv 8.3E-03; 2.8E-05 6
rs1374051619
ELAC2
0.827 0.080 17 12995026 missense variant C/G snv 4.0E-06 5
rs1870050
GLDN
0.827 0.160 15 51344354 intron variant A/C snv 6.0E-02 5
rs765521022
KLK3
0.851 0.080 19 50858171 missense variant T/C snv 4
rs544190
PCA3 ; PRUNE2
0.851 0.080 9 76763591 intron variant G/A snv 0.32 4
rs11017056
C10orf143
1.000 0.080 10 130032376 intron variant A/C;T snv 0.21 3
rs56350726
SLC28A3 ; LOC105376116
0.882 0.080 9 84285454 missense variant T/A;C snv 7.2E-02; 1.2E-05 3
rs2208532
SRD5A2
0.882 0.080 2 31563919 intron variant G/A snv 0.59 3
rs676033
SRD5A2
0.882 0.080 2 31583901 upstream gene variant T/C snv 0.69 3
rs875858
VAC14
1.000 0.080 16 70741552 intron variant C/A;T snv 3
rs12030724
YBX1
0.925 0.080 1 42694347 intron variant A/T snv 8.9E-02 2
rs549654942
HGF
1.000 0.080 7 81729639 missense variant C/T snv 2.0E-05 7.0E-06 1
rs868955734
LIMK1
1.000 0.080 7 74107928 stop gained G/A;T snv 1.6E-05 1
rs748636101
PAK4
1.000 0.080 19 39173897 missense variant G/A snv 8.2E-06 7.0E-06 1
rs753495682
PDLIM5
1.000 0.080 4 94618065 missense variant G/A snv 2.4E-05 7.0E-06 1