Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587776650
NBN
0.790 0.280 8 89971214 frameshift variant GTTTT/- delins 2.0E-04 11
rs80357796
BRCA1
0.752 0.240 17 43094464 frameshift variant T/- del 11
rs3020450
ESR2
0.807 0.200 14 64301584 splice region variant C/A;T snv 10
rs11651755
HNF1B
0.763 0.160 17 37739849 intron variant T/C snv 0.52 9
rs1256031
ESR2
0.790 0.200 14 64279461 intron variant G/A;T snv 0.57 9
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 9
rs4648068
NFKB1
0.790 0.240 4 102597148 intron variant A/G snv 0.31 9
rs80356952
BRCA1
0.790 0.200 17 43093901 stop gained G/A snv 9
rs11655505
NBR2 ; BRCA1
0.776 0.160 17 43126360 intron variant G/A snv 0.31 8
rs2304277
OGG1 ; CAMK1
0.776 0.280 3 9759396 non coding transcript exon variant G/A snv 0.26 8
rs2665390
LOC107986148 ; TIPARP
0.776 0.160 3 156679960 intron variant C/T snv 0.92 8
rs587778617
PMS2
0.807 0.240 7 5987504 stop gained G/A snv 7.0E-06 8
rs80357115
BRCA1
0.790 0.200 17 43092597 stop gained A/C;T snv 8
rs80357750
BRCA1
0.790 0.200 17 43115759 frameshift variant G/- delins 8
rs8037137
RCCD1
0.807 0.160 15 90963407 upstream gene variant T/C snv 0.19 8
rs1243180
MLLT10
0.790 0.160 10 21626690 intron variant T/A snv 0.23 7
rs1467465
THEMIS2
0.827 0.160 1 27884892 non coding transcript exon variant A/G snv 0.61 7
rs1469713
GATAD2A
0.827 0.160 19 19417997 intron variant A/G snv 0.44 7
rs1801200
ERBB2
0.790 0.200 17 39723335 missense variant A/G;T snv 7
rs6917
PHB
0.790 0.200 17 49404181 3 prime UTR variant G/A snv 0.16 7
rs7937840
INCENP
0.807 0.200 11 62126500 intron variant C/T snv 0.20 7
rs886039920
BRCA1
0.807 0.160 17 43115755 frameshift variant ACAGG/- delins 7
rs1131691022
TP53
0.827 0.160 17 7670685 frameshift variant GG/A;G delins 6
rs1256030
ESR2
0.827 0.240 14 64280452 intron variant A/G;T snv 6
rs1836724
ERBB4
0.807 0.240 2 211380227 3 prime UTR variant G/A snv 0.57 6