Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4281481
CCDC179 ; GAS2
0.882 0.080 11 22859013 intron variant C/G snv 0.36 3
rs161740
CHD1
0.882 0.200 5 98869326 intron variant C/A;T snv 3
rs17089362
CNDP2
0.882 0.160 18 74518403 non coding transcript exon variant G/A;T snv 3
rs890336
CNDP2
0.882 0.160 18 74520377 3 prime UTR variant C/G;T snv 3
rs281874762
COL4A5
0.882 0.160 X 108578114 stop gained G/A;T snv 5.5E-06 3
rs11571317
CTLA4
0.882 0.160 2 203867285 upstream gene variant C/T snv 5.2E-02 3
rs926632
EDN3
0.882 0.160 20 59309707 intron variant C/T snv 0.61 3
rs1033182
ESR1
0.882 0.160 6 151873899 intron variant G/A snv 0.26 3
rs1709183
ESR1
0.882 0.160 6 151872861 intron variant C/T snv 0.67 3
rs2431260
ESR1
0.882 0.160 6 151871196 intron variant G/C;T snv 3
rs267607183
INF2
0.882 0.080 14 104703440 missense variant G/A snv 3
rs2032487
MYH9
0.882 0.080 22 36299382 intron variant C/T snv 0.78 3
rs35238405
NPHS1
0.882 0.080 19 35849565 missense variant T/C snv 8.0E-04 2.6E-03 3
rs1057518923
PKD1
0.925 0.200 16 2115395 frameshift variant -/C delins 3
rs148812376
PKD1
0.882 0.120 16 2099955 missense variant G/A snv 1.7E-04 3.2E-04 3
rs2575390
PRKCB
0.925 0.080 16 23835433 upstream gene variant G/A;C snv 3
rs3760106
PRKCB
0.925 0.080 16 23834475 upstream gene variant C/T snv 0.23 3
rs2720709
PVT1
0.882 0.160 8 128046110 intron variant G/A;C snv 3
rs41302867
RREB1
0.925 0.080 6 7240643 intron variant G/A snv 8.5E-02 8.2E-02 3
rs12434215
RTN1
0.882 0.160 14 59642862 intron variant A/G snv 0.33 3
rs1952034
RTN1
0.882 0.160 14 59691018 intron variant C/T snv 0.35 3
rs1749824
ZMIZ1
0.925 0.080 10 79164105 intron variant C/A snv 0.39 3
rs743811 0.882 0.160 22 35396981 upstream gene variant T/A;C snv 4
rs867394500
ACE
0.851 0.080 17 63477301 missense variant G/T snv 4
rs121908529
AGXT
0.851 0.160 2 240871433 missense variant G/A;C snv 5.6E-04 4