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
rs863223301
TP53
0.925 0.080 17 7675130 frameshift variant -/CCATGGC delins 2
rs12951053
TP53
0.732 0.160 17 7674089 intron variant A/C snv 0.10 14
rs587781705
CHEK2
0.851 0.200 22 28734506 stop gained A/C snv 5
rs121913282
PIK3CA
0.882 0.040 3 179221072 missense variant A/C snv 4
rs7591996 0.882 0.040 2 6321289 intron variant A/C snv 0.57 3
rs29001322
MMS19
0.882 0.040 10 97462918 non coding transcript exon variant A/C;G snv 3
rs770771727
UTRN
0.882 0.040 6 144751941 missense variant A/C;G snv 4.5E-05; 2.5E-05 3
rs560596101
CHEK2
0.851 0.200 22 28725241 splice donor variant A/C;G;T snv 4.0E-06 5
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs8103992 0.882 0.040 19 19554834 regulatory region variant A/C;T snv 3
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs6218
LINC02456 ; HELLPAR ; IGF1
0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02 13
rs367597251
MDM2
0.807 0.080 12 68839587 missense variant A/G snv 1.5E-04 5.1E-04 10
rs7023329
MTAP
0.790 0.160 9 21816529 intron variant A/G snv 0.50 9
rs1989839
ZMYND10 ; RASSF1
0.790 0.160 3 50341515 intron variant A/G snv 0.22 0.20 8
rs9895829
TP53
0.807 0.080 17 7675361 5 prime UTR variant A/G snv 7.4E-02 6
rs10208273 0.882 0.040 2 6383862 intergenic variant A/G snv 0.30 3
rs1061970
COL1A1
0.882 0.040 17 50184491 3 prime UTR variant A/G snv 0.13 3
rs780673045
MDM2
0.882 0.040 12 68839592 missense variant A/G snv 1.2E-05 3
rs998075
IGF2R
0.882 0.040 6 160047246 synonymous variant A/G snv 0.53 0.54 3