Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5844572
MIF ; MIF-AS1
0.752 0.360 22 23893562 intron variant -/ATTC delins 11
rs371194629
HLA-G
0.790 0.320 6 29830804 3 prime UTR variant -/ATTTGT;ATTTGTTCACGCCT;ATTTGTTCATGCCT ins 8
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs70991108
MSH3 ; DHFR
0.807 0.280 5 80654344 intron variant -/TCGCGCGTCCCGCCCAGGT;TGGCGCGTCCCGCCCAGGT ins 0.51 6
rs1414323823
CYP1A1
0.851 0.160 15 74722772 frameshift variant -/TCTCGGT ins 4.0E-06 4
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 16
rs1341239
PRL ; CASC15
0.776 0.360 6 22303975 intron variant A/C snv 0.65 8
rs6568431
ATG5
0.790 0.320 6 106140931 intron variant A/C snv 0.61 7
rs729302 0.827 0.160 7 128928906 intergenic variant A/C snv 0.28 6
rs10489265
TNFSF4 ; LOC100506023
0.827 0.200 1 173266926 regulatory region variant A/C snv 0.21 5
rs1517352
STAT4
0.851 0.160 2 191066738 intron variant A/C snv 0.45 5
rs2523987
TRIM31-AS1 ; TRIM31
0.827 0.280 6 30112216 intron variant A/C snv 9.2E-02 5
rs6659932
IL12RB2
0.827 0.240 1 67336688 intron variant A/C snv 0.81 5
rs437179
SKIV2L ; CYP21A2
0.882 0.160 6 31961237 missense variant A/C snv 0.76 0.78 3
rs630379
NELFE ; CYP21A2
0.882 0.200 6 31954477 intron variant A/C snv 0.77 0.79 3
rs10498070 0.925 0.080 2 219833404 intergenic variant A/C snv 0.39 2
rs1891385
IL33
0.925 0.120 9 6219845 intron variant A/C snv 0.10 2
rs3181032
IFNG-AS1
0.925 0.160 12 68162395 intron variant A/C snv 5.3E-02 2
rs7172677 0.925 0.080 15 75132252 intergenic variant A/C snv 0.71 2
rs13280095
PVT1
1.000 0.080 8 128166844 intron variant A/C snv 0.26 1
rs1419183
ZSCAN26
1.000 0.080 6 28275017 intron variant A/C snv 0.17 1
rs1734787
MECP2
1.000 0.080 X 154059995 non coding transcript exon variant A/C snv 0.17 1
rs180977001
PXK
1.000 0.080 3 58332737 upstream gene variant A/C snv 4.4E-02 1
rs3136744
POLB
1.000 0.080 8 42349829 intron variant A/C snv 9.5E-02 1