Disease: Malignant neoplasm of breast
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs10931936
CASP8
0.827 0.120 2 201279205 intron variant T/C snv 0.72 6
rs11225395
MMP8
0.776 0.360 11 102725749 intron variant A/C;G snv 11
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs16953002
FTO
0.882 0.080 16 54080912 intron variant G/A snv 0.19 5
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs2242652
TERT
0.724 0.400 5 1279913 intron variant G/A snv 0.18 16
rs2284378
RALY
0.851 0.080 20 34000289 intron variant T/C;G snv 4
rs28362491
LOC105377621 ; NFKB1
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 29
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs3834129
CASP8
0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs387906659
AKT2
0.742 0.280 19 40257052 stop gained C/A;T snv 14
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs397514606
AKT3
0.763 0.320 1 243695714 missense variant C/T snv 14
rs397517132
EGFR
0.623 0.280 7 55191846 missense variant A/T snv 48
rs401618
HLA-A
0.827 0.120 6 29982433 downstream gene variant A/G;T snv 5
rs4516035
VDR
0.776 0.360 12 47906043 non coding transcript exon variant T/C snv 0.31 10
rs4950928
CHI3L1
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs927650
CYP24A1
0.763 0.240 20 54156202 intron variant T/A;C snv 9
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614