Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs112417755
GATA3
1.000 0.080 10 8073738 splice acceptor variant G/C;T snv 1
rs515299
CFH
0.925 0.080 1 196737547 missense variant G/A;C;T snv 4.8E-05; 1.7E-02 4
rs1057518923
PKD1
0.925 0.200 16 2115395 frameshift variant -/C delins 3
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
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
rs41302867
RREB1
0.925 0.080 6 7240643 intron variant G/A snv 8.5E-02 8.2E-02 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
rs16347
IL1A
0.925 0.080 2 112774138 3 prime UTR variant -/TGAA delins 0.70 2
rs17709344
LOC107983974
0.925 0.080 15 93608310 intron variant G/A snv 4.0E-02 2
rs183962941
UMOD
0.925 0.080 16 20343125 intron variant G/A snv 1.1E-02 2
rs2391335
EFNB2
0.925 0.080 13 106519637 non coding transcript exon variant T/C;G snv 0.50 2
rs2413396
MYH9
0.925 0.080 22 36312039 intron variant C/G;T snv 0.88 2