Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2897075
ZKSCAN1
1.000 0.040 7 100032719 intron variant C/T snv 0.31 1
rs57942103
ZFPM2
1.000 0.040 8 105501233 intron variant A/C snv 0.25 3
rs1327135247
ZEB1
0.827 0.160 10 31510820 missense variant C/T snv 4.0E-06 5
rs1487151044
ZEB1
0.851 0.080 10 31510817 missense variant T/C snv 5
rs4143333
ZDHHC20P2
1.000 0.040 6 31380742 non coding transcript exon variant A/G snv 7.9E-02 1
rs71636784
ZDHHC18
1.000 0.040 1 26842709 intron variant T/G snv 0.12 4
rs7650602
ZBTB38
1.000 0.040 3 141428572 intron variant T/C snv 0.51 2
rs207936
XRCC5
1.000 0.040 2 216175310 non coding transcript exon variant C/T snv 0.24 1
rs3821104
XRCC5
1.000 0.040 2 216193123 intron variant G/A snv 0.72 1
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs569444
WTAPP1 ; MMP3
0.925 0.120 11 102836574 non coding transcript exon variant G/A;T snv 0.12; 6.7E-06 0.10 3
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs2071230
WTAPP1 ; MMP1
0.882 0.080 11 102790228 3 prime UTR variant A/G snv 0.15 3
rs499459
WTAPP1
0.925 0.080 11 102822455 intron variant A/G snv 0.90 3
rs564018
WTAPP1
0.925 0.080 11 102820688 intron variant A/G;T snv 3
rs470234
WTAPP1
1.000 0.040 11 102811075 intron variant T/A;G snv 2
rs470292
WTAPP1
1.000 0.040 11 102814664 intron variant C/A snv 0.90 2
rs470928
WTAPP1
1.000 0.040 11 102814649 intron variant G/A;T snv 2
rs473238
WTAPP1
1.000 0.040 11 102829629 intron variant T/C snv 0.90 2
rs475937
WTAPP1
1.000 0.040 11 102816969 intron variant A/C;T snv 2
rs505987
WTAPP1
1.000 0.040 11 102815179 intron variant A/G snv 0.89 2
rs520146
WTAPP1
1.000 0.040 11 102819400 intron variant T/C snv 0.90 2
rs525119
WTAPP1
1.000 0.040 11 102831415 intron variant G/T snv 0.90 2
rs553542
WTAPP1
1.000 0.040 11 102830645 intron variant C/T snv 0.90 2
rs593698
WTAPP1
1.000 0.040 11 102833745 intron variant G/A snv 0.10 2