Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs3025058
MMP3
0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs139016349
MRAS
1.000 0.040 3 138380319 intron variant -/CTT delins 0.21 1
rs3045215
IRF2BP2
0.882 0.040 1 234605171 3 prime UTR variant -/GTTACAATA;GTTATAATA delins 3
rs3217713
NFKBIZ
1.000 0.040 3 101857185 splice region variant -/TTCTAGAAAGCTTTAATAACCAC;TTTTAGAAAGCTTTAATAACCAC;TTTTTAGAAAGCTTTAATAACCAC delins 0.81 1
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs34091558
LMOD1
1.000 0.040 1 201917642 intron variant A/- delins 0.25 2
rs528732638
CHST9 ; AQP4-AS1
0.851 0.120 18 26940224 intron variant A/-;AA;AAA;AAAA delins 5
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs2239704
LTA ; LOC100287329
0.732 0.320 6 31572364 5 prime UTR variant A/C snv 0.64 17
rs4646
MIR4713HG ; CYP19A1
0.716 0.360 15 51210647 3 prime UTR variant A/C snv 0.67 0.70 16
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 10
rs12440045 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 6
rs3761581
APLN
0.851 0.160 X 129655744 upstream gene variant A/C snv 0.11 5
rs7248488
ZNF208
0.851 0.160 19 22005907 intron variant A/C snv 0.59 5
rs4919686
WBP1L ; CYP17A1 ; CYP17A1-AS1
0.851 0.200 10 102832492 3 prime UTR variant A/C snv 0.23 0.21 4
rs585967 1.000 0.040 2 21047682 upstream gene variant A/C snv 0.81 4
rs606452
SERPINH1
1.000 0.040 11 75565133 intron variant A/C snv 0.78 4
rs8089
LOC101929523 ; THBS2
0.851 0.080 6 169217631 splice region variant A/C snv 0.22 4
rs8103163
ZNF208
0.882 0.120 19 21991950 intron variant A/C snv 0.59 4
rs12115090
CRISPLD1
0.882 0.040 8 75012585 intron variant A/C snv 0.33 0.44 3
rs55791371
SMARCA4
0.925 0.080 19 11077477 intron variant A/C snv 0.11 3
rs9515201
COL4A2
0.925 0.080 13 110388451 intron variant A/C snv 0.63 3
rs11072811
MORF4L1
1.000 0.040 15 78839988 intron variant A/C snv 0.51 2