Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs753350907
PAX2
0.827 0.080 10 100806499 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 5
rs515299
CFH
0.925 0.080 1 196737547 missense variant G/A;C;T snv 4.8E-05; 1.7E-02 4
rs867394500
ACE
0.851 0.080 17 63477301 missense variant G/T snv 4
rs1162592300
ALB
0.925 0.080 4 73412045 missense variant G/A snv 3
rs1749824
ZMIZ1
0.925 0.080 10 79164105 intron variant C/A snv 0.39 3
rs2032487
MYH9
0.882 0.080 22 36299382 intron variant C/T snv 0.78 3
rs2575390
PRKCB
0.925 0.080 16 23835433 upstream gene variant G/A;C snv 3
rs267607183
INF2
0.882 0.080 14 104703440 missense variant G/A snv 3
rs35238405
NPHS1
0.882 0.080 19 35849565 missense variant T/C snv 8.0E-04 2.6E-03 3
rs3759126
AQP2
0.882 0.080 12 49950079 upstream gene variant A/G snv 0.23 3
rs3760106
PRKCB
0.925 0.080 16 23834475 upstream gene variant C/T snv 0.23 3
rs41302867
RREB1
0.925 0.080 6 7240643 intron variant G/A snv 8.5E-02 8.2E-02 3
rs4281481
CCDC179 ; GAS2
0.882 0.080 11 22859013 intron variant C/G snv 0.36 3
rs10137082
IL25
0.925 0.080 14 23370824 upstream gene variant C/T snv 0.23 2
rs10404257
ACTN4
0.925 0.080 19 38645846 upstream gene variant G/A snv 0.50 2
rs10808565
PVT1
0.925 0.080 8 127995166 non coding transcript exon variant C/T snv 0.31 2
rs11089781
APOL3
0.925 0.080 22 36160720 stop gained G/A snv 1.6E-02 6.5E-02 2
rs115489112
NPHS1
0.925 0.080 19 35830918 missense variant G/A snv 4.3E-04 1.6E-03 2
rs12137135 0.925 0.080 1 22348728 intergenic variant A/C;G snv 2
rs12431381
RTN1
0.925 0.080 14 59643053 intron variant T/C snv 0.35 2
rs12437854
LOC107983974
0.925 0.080 15 93598604 intron variant T/G snv 0.10 2
rs12917114 0.925 0.080 15 47852953 intron variant C/T snv 8.9E-02 2
rs145640112
KLKB1
0.925 0.080 4 186250267 missense variant A/C;G snv 1.8E-04; 4.0E-06 2
rs146400394
NPHS1
0.925 0.080 19 35842486 missense variant C/T snv 6.8E-05 4.9E-05 2
rs1516792
IL1A
0.925 0.080 2 112778356 intron variant G/A snv 2