Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11554137
IDH1
0.742 0.040 2 208248468 synonymous variant G/A snv 5.1E-02 6.8E-02 13
rs1482518887
RUNX1
0.790 0.040 21 34887018 missense variant C/T snv 7.0E-06 8
rs1801020
GRK6 ; F12 ; SLC34A1
1.000 0.040 5 177409531 5 prime UTR variant A/G snv 0.65 0.67 8
rs138817062
PML
0.882 0.040 15 74044940 missense variant C/T snv 4.0E-05 7.0E-06 4
rs35602083
FLT3
0.851 0.040 13 28049450 missense variant C/T snv 1.7E-02 1.6E-02 4
rs3842803
PTGS1
0.925 0.040 9 122392256 synonymous variant T/C snv 2.4E-02 8.2E-02 4
rs652722
PAX6-AS1 ; PAUPAR
1.000 0.040 11 31883988 intron variant C/T snv 0.32 4
rs12133576
DR1
1.000 0.040 1 93350843 intron variant A/G snv 0.51 3
rs12199222
NUP153
1.000 0.040 6 17699091 intron variant G/A;T snv 3
rs17036328
PPARG
1.000 0.040 3 12348985 intron variant T/C snv 0.14 3
rs17056278
EBF1
0.925 0.040 5 158825430 intron variant C/G snv 5.3E-02 3
rs17806888
SUCLG2
1.000 0.040 3 67365898 intron variant T/C snv 9.1E-02 3
rs212090
ABCC1
1.000 0.040 16 16142147 3 prime UTR variant T/A snv 0.36 3
rs2270859
LOC105374071 ; PARP9
1.000 0.040 3 122536861 non coding transcript exon variant G/A snv 0.14 3
rs233112
DDAH1
0.925 0.040 1 85320068 3 prime UTR variant T/C snv 0.37 3
rs2597513 1.000 0.040 3 13514336 regulatory region variant C/T snv 0.88 3
rs3213409
JAK3
0.925 0.040 19 17834887 missense variant C/T snv 8.6E-03 7.3E-03 3
rs478093
PHGDH ; LOC105378937
1.000 0.040 1 119712503 5 prime UTR variant A/G snv 0.73 3
rs4969178
PGS1
1.000 0.040 17 78392121 intron variant A/G snv 0.63 3
rs4969186
PGS1
1.000 0.040 17 78402323 intron variant G/C snv 0.62 3
rs602074
PAUPAR
1.000 0.040 11 31900616 intron variant C/T snv 0.46 3
rs6088343 1.000 0.040 20 33908259 downstream gene variant C/T snv 0.46 3
rs6142044 1.000 0.040 20 33918789 intergenic variant A/T snv 0.47 3
rs6489785 1.000 0.040 12 120925921 TF binding site variant T/C snv 0.68 3
rs683028
PAUPAR
1.000 0.040 11 31901029 intron variant A/G snv 0.44 3