Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6785617 0.882 0.120 3 172501054 downstream gene variant A/T snv 3.7E-02 4
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs874945 0.732 0.240 12 53961667 upstream gene variant C/T snv 0.38 14
rs3760396
CCL2
0.732 0.280 17 34254422 upstream gene variant G/C snv 0.15 13
rs8037137
RCCD1
0.807 0.160 15 90963407 upstream gene variant T/C snv 0.19 8
rs3814113 0.827 0.200 9 16915023 upstream gene variant T/C snv 0.41 5
rs67397200 0.827 0.160 19 17290595 upstream gene variant C/G snv 0.27 5
rs7246045
CGB5
0.882 0.120 19 49042825 upstream gene variant T/G snv 2.9E-02 5
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs267607911
MSH2
0.851 0.200 2 47403192 start lost A/C;G;T snv 5.1E-05; 1.4E-05 8
rs904571820
ESR1
0.851 0.160 6 151842664 start lost A/G snv 4.0E-06 5
rs3020450
ESR2
0.807 0.200 14 64301584 splice region variant C/A;T snv 10
rs876660702
BRCA1
0.851 0.160 17 43063333 splice region variant C/T snv 4
rs7526063
MTR
0.882 0.120 1 236808698 splice region variant C/T snv 3.8E-02 5.6E-02 3
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
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
rs80357750
BRCA1
0.790 0.200 17 43115759 frameshift variant G/- delins 8
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
rs63750695
PMS2
0.851 0.280 7 5978675 frameshift variant AAGTT/- delins 6
rs587781803
BRCA2
0.851 0.200 13 32341169 frameshift variant AAGAG/- delins 5
rs80357517
BRCA1
0.827 0.200 17 43092277 frameshift variant -/T delins 5
rs80357669
BRCA1
0.851 0.200 17 43093074 frameshift variant G/- delins 5