Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9974610 1.000 0.080 21 31646056 intergenic variant A/G snv 0.13 3
rs9932581
MVD ; CYBA
16 88651945 3 prime UTR variant C/T snv 0.39 1
rs9896208
ACE
17 63498748 intron variant T/C snv 0.57 1
rs9357155
PSMB8
1.000 0.120 6 32842071 non coding transcript exon variant G/A;C snv 2
rs9275596 0.827 0.280 6 32713854 upstream gene variant C/T snv 0.66 7
rs9275424 6 32702799 downstream gene variant A/G snv 0.30 1
rs9275224 0.851 0.200 6 32692101 TF binding site variant A/G snv 0.53 5
rs8731
GPN1 ; SUPT7L
2 27650459 3 prime UTR variant C/G snv 0.22 1
rs869025495
NPHS2
0.851 0.080 1 179564715 missense variant G/A snv 6
rs868580411
COL4A5
1.000 X 108602973 missense variant G/A;T snv 2
rs841853
SLC2A1
0.882 0.200 1 42935767 intron variant A/C snv 0.66 4
rs8192678
PPARGC1A
0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs8177412
GPX3 ; LOC105378228
0.851 0.160 5 151020526 5 prime UTR variant T/C snv 0.15 5
rs7947841
CAT
11 34470133 intron variant G/A snv 1.0E-01 1
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs776400293
TLR3
4 186076620 start lost A/G snv 4.0E-06 7.0E-06 1
rs7704116
PPP2CA
1.000 0.080 5 134216763 intron variant C/T snv 9.9E-02 2
rs763059810
CXCR4
0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs758564400
REN
0.925 0.120 1 204156683 missense variant A/G snv 4.0E-06 5
rs74421874
PSMD9
0.776 0.360 12 121902546 non coding transcript exon variant G/A snv 0.24 14
rs741301
ELMO1
0.925 0.160 7 36878390 intron variant C/T snv 0.59 3
rs739401
CARS1
11 3015094 intron variant C/T snv 0.45 2
rs713041
GPX4
0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs702553
PDE4D
0.882 0.160 5 60440946 intron variant A/T snv 0.37 6
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134