Disease: Malignant neoplasm of breast
Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 19
rs1011970
CDKN2B-AS1
0.677 0.320 9 22062135 intron variant G/T snv 0.23 18
rs10472076 0.925 0.080 5 58888234 regulatory region variant T/A;C snv 2
rs10759243 0.925 0.080 9 107543834 upstream gene variant C/A;T snv 2
rs10771399 0.827 0.080 12 28002147 intergenic variant A/G snv 8.9E-02 3
rs10822013
ZNF365
0.851 0.080 10 62492218 intron variant C/T snv 0.42 2
rs10941679 0.763 0.120 5 44706396 intergenic variant A/G snv 0.25 2
rs10995190
ZNF365
0.882 0.080 10 62518923 intron variant G/A snv 0.16 3
rs11075995
FTO
0.882 0.080 16 53821379 intron variant A/T snv 0.77 2
rs11199914 0.925 0.080 10 121334387 intergenic variant C/T snv 0.40 2
rs11242675 0.925 0.080 6 1318643 downstream gene variant C/T snv 0.58 2
rs11249433
EMBP1
0.827 0.160 1 121538815 intron variant A/C;G snv 3
rs1154865 0.882 0.160 12 73596057 intergenic variant C/G snv 0.22 3
rs11552449
AP4B1 ; DCLRE1B
0.925 0.080 1 113905767 missense variant C/G;T snv 0.22 0.15 2
rs11571833
BRCA2
0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 21
rs11780156
PVT1
0.925 0.080 8 128182395 intron variant C/T snv 0.13 2
rs11814448 0.925 0.080 10 22026914 intergenic variant A/C snv 0.21 2
rs11820646 0.925 0.080 11 129591276 upstream gene variant T/C;G snv 2
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 3
rs12422552 0.925 0.080 12 14260997 regulatory region variant G/C snv 0.30 3
rs12493607
TGFBR2
0.882 0.080 3 30641447 intron variant G/C;T snv 2
rs12710696
LINC01376
0.925 0.080 2 19121042 intron variant T/A;C snv 2
rs12906542
ADAMTS7P3
0.925 0.080 15 77977130 intron variant A/C;G;T snv 2
rs1292011
LOC105370003
0.851 0.080 12 115398717 regulatory region variant A/G snv 0.43 2
rs12922061
CASC16
0.925 0.080 16 52601088 intron variant C/T snv 0.19 2