Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs281865157
WRN
1.000 0.080 8 31108591 intron variant A/C;G snv 1
rs17847577
WRN
0.925 0.120 8 31081132 stop gained C/T snv 1.7E-04 3.2E-04 2
rs1198210848
WRN
1.000 0.080 8 31058535 stop gained G/T snv 4.0E-06 7.0E-06 1
rs121908446
WRN
1.000 0.080 8 31157461 stop gained C/T snv 2.0E-05 2.1E-05 1
rs121908447
WRN
1.000 0.080 8 31147397 stop gained C/T snv 1
rs1303126572
WRN
1.000 0.080 8 31157509 stop gained C/T snv 7.0E-06 1
rs143916053
WRN
1.000 0.080 8 31111720 stop gained C/T snv 1.6E-05 7.0E-06 1
rs1554527775
WRN
1.000 0.080 8 31116412 stop gained C/T snv 1
rs1554528411
WRN
1.000 0.080 8 31120398 stop gained G/A snv 1
rs1563331288
WRN
1.000 0.080 8 31067082 stop gained T/G snv 1
rs1563338837
WRN
1.000 0.080 8 31081138 stop gained G/T snv 1
rs1563357741
WRN
1.000 0.080 8 31111696 stop gained C/T snv 1
rs1563376347
WRN
1.000 0.080 8 31141456 stop gained T/A snv 1
rs1563376526
WRN
1.000 0.080 8 31141564 stop gained T/G snv 1
rs370324188
WRN
1.000 0.080 8 31068276 stop gained C/T snv 8.2E-06 7.0E-06 1
rs371538747
WRN
1.000 0.080 8 31064406 stop gained T/A;C;G snv 4.0E-06 1
rs747319628
WRN
1.000 0.080 8 31132498 stop gained C/T snv 1.6E-05 2.8E-05 1
rs757808169
WRN
1.000 0.080 8 31090857 stop gained C/T snv 4.0E-06 1
rs763089663
WRN
1.000 0.080 8 31111747 stop gained C/T snv 8.0E-06 1
rs774765029
WRN
1.000 0.080 8 31124556 stop gained C/T snv 2.4E-05 1
rs1346044
WRN
0.708 0.440 8 31167138 missense variant T/C snv 0.24 0.23 23
rs2230009
WRN
0.827 0.240 8 31064419 missense variant G/A snv 5.8E-02 7.8E-02 5
rs188554751
WRN
0.851 0.200 8 31120403 missense variant C/T snv 4.0E-06 4
rs3087425
WRN
0.882 0.160 8 31120294 missense variant C/T snv 2.8E-03 8.7E-04 3
rs121908448
WRN
1.000 0.080 8 31090843 missense variant A/T snv 1