Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62
rs58598099
PKD1
0.882 0.200 16 2116917 missense variant A/G snv 3
rs11122577
AGT
1.000 0.120 1 230711810 intron variant C/A snv 0.19 2
rs121918040
PKD2
0.925 0.120 4 88065479 stop gained C/T snv 7.0E-06 2
rs121918043
PKD2
0.925 0.120 4 88046854 missense variant A/T snv 2
rs1249050389
PTCH1
0.925 0.240 9 95485696 stop gained G/C snv 2
rs1302726543
PKD2
0.925 0.120 4 88019499 stop gained C/T snv 7.0E-06 2
rs1464816
REN
1.000 0.120 1 204159726 intron variant T/C;G snv 2
rs1553925453
PKD2
0.925 0.120 4 88038371 missense variant C/T snv 2
rs1187336837
PKD2
1.000 0.120 4 88007931 frameshift variant C/-;CC delins 1
rs1232369409
PKD2
1.000 0.120 4 88008244 frameshift variant G/- delins 7.0E-06 1
rs1392093609
PKD2
1.000 0.120 4 88007759 missense variant C/T snv 1
rs1553926509
PKD2
1.000 0.120 4 88052018 frameshift variant TA/- delins 1
rs1553926905
PKD2
1.000 0.120 4 88056143 stop gained C/T snv 1
rs1553927080
PKD2
1.000 0.120 4 88058104 splice donor variant G/A snv 1
rs1555452849
MIR6511B1 ; PKD1
1.000 0.120 16 2106172 frameshift variant G/- delins 1
rs1560592253
PKD2
1.000 0.120 4 88008174 frameshift variant G/- delins 1
rs750723025
GANAB ; INTS5
1.000 0.120 11 62646584 inframe deletion TACCGC/- delins 7.0E-06 1
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1391596181
PKD2
1.000 0.120 4 88046647 stop gained T/A;C snv 4.0E-06 1
rs886041114
PKD2
1.000 0.120 4 88046642 missense variant G/A;T snv 4.0E-06 2
rs749004212
PKD2
1.000 0.120 4 88038365 stop gained C/T snv 4.0E-06 1.4E-05 1
rs746231889
PRKCSH
1.000 0.120 19 11447152 missense variant C/A;G;T snv 4.0E-06; 1.9E-04 1
rs1487813753
PKD2L1
1.000 0.120 10 100293336 missense variant T/C;G snv 8.0E-06 1
rs1131692280
PKD2
0.925 0.120 4 88043458 splice donor variant G/A snv 8.0E-06 1.4E-05 3