Disease: Breast Carcinoma
Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10090154 0.807 0.160 8 127519892 intergenic variant T/A;C snv 7
rs10165970
NPAS2
0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs10204525
PDCD1
0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 20
rs1044129
AVEN ; RYR3
0.790 0.200 15 33866065 3 prime UTR variant A/G;T snv 9
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 19
rs10506868
VTI1A
0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 8
rs10519097
RORA
0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs11196067
VTI1A
0.752 0.160 10 112709306 intron variant A/T snv 0.32 10
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13 10
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 213
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 28
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 45
rs11685387
XRCC5
0.776 0.240 2 216109091 splice region variant C/T snv 0.30 9
rs11943456
TMEM165
0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 45
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62
rs12241008
VTI1A
0.716 0.160 10 112520943 intron variant T/C snv 0.13 8
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 26
rs1258159645
NQO1
0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs12778366
SIRT1
0.724 0.480 10 67883321 upstream gene variant T/C;G snv 13
rs13347
CD44
0.763 0.320 11 35231725 3 prime UTR variant C/A;T snv 12
rs14133
HSPB2-C11orf52 ; CRYAB ; HSPB2
0.807 0.200 11 111911973 5 prime UTR variant G/C snv 0.27 7