Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs145640112
KLKB1
0.925 0.080 4 186250267 missense variant A/C;G snv 1.8E-04; 4.0E-06 2
rs4253373
KLKB1
0.925 0.080 4 186250250 missense variant C/A snv 6.7E-04 2.5E-03 2
rs301640
LINC01442
0.925 0.080 13 60885853 intron variant C/G;T snv 2
rs12437854
LOC107983974
0.925 0.080 15 93598604 intron variant T/G snv 0.10 2
rs17709344
LOC107983974
0.925 0.080 15 93608310 intron variant G/A snv 4.0E-02 2
rs9395890
MLIP ; LOC101927189
0.925 0.080 6 53956196 intron variant G/A;T snv 2
rs9298190
MSC-AS1
0.925 0.080 8 71932099 intron variant T/C snv 0.36 2
rs2413396
MYH9
0.925 0.080 22 36312039 intron variant C/G;T snv 0.88 2
rs115489112
NPHS1
0.925 0.080 19 35830918 missense variant G/A snv 4.3E-04 1.6E-03 2
rs146400394
NPHS1
0.925 0.080 19 35842486 missense variant C/T snv 6.8E-05 4.9E-05 2
rs10808565
PVT1
0.925 0.080 8 127995166 non coding transcript exon variant C/T snv 0.31 2
rs6954996
RAC1
0.925 0.080 7 6401627 non coding transcript exon variant G/A;T snv 2
rs702483
RAC1
0.925 0.080 7 6387310 intron variant C/A;T snv 0.54 2
rs836488
RAC1
0.925 0.080 7 6380162 intron variant C/T snv 0.13 2
rs9374
RAC1
0.925 0.080 7 6402740 3 prime UTR variant G/A snv 0.18 2
rs12431381
RTN1
0.925 0.080 14 59643053 intron variant T/C snv 0.35 2
rs2802723
SDCCAG8
0.925 0.080 1 243335010 intron variant T/C;G snv 2
rs2838302
SIK1
0.925 0.080 21 43419273 intron variant A/G snv 1.0E-01 2
rs183962941
UMOD
0.925 0.080 16 20343125 intron variant G/A snv 1.1E-02 2
rs12197043 0.882 0.160 6 149130141 regulatory region variant A/G snv 0.37 3
rs1670754 0.882 0.160 4 32263375 intergenic variant G/A snv 0.24 3
rs4897081 0.882 0.160 6 149115402 upstream gene variant G/A;T snv 3
rs8014363 0.882 0.160 14 53964857 downstream gene variant C/T snv 0.61 3
rs1162592300
ALB
0.925 0.080 4 73412045 missense variant G/A snv 3
rs3759126
AQP2
0.882 0.080 12 49950079 upstream gene variant A/G snv 0.23 3