Disease: Malignant neoplasm of breast
Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
rs11552449
AP4B1 ; DCLRE1B
0.925 0.080 1 113905767 missense variant C/G;T snv 0.22 0.15 2
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
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
rs132390
LOC105372985 ; EMID1
0.925 0.080 22 29225488 intron variant C/T snv 0.96 2
rs13329835
CDYL2
0.925 0.080 16 80616908 intron variant A/G snv 0.35 2
rs1353747
PDE4D
0.882 0.080 5 59041654 intron variant T/G snv 6.9E-02 3
rs1357245
NEK10
0.925 0.080 3 27145111 intron variant C/T snv 0.35 2
rs1432679
EBF1
0.851 0.080 5 158817075 intron variant C/T snv 0.44 2
rs1436904
AQP4-AS1 ; CHST9
0.851 0.080 18 26990703 intron variant T/G snv 0.35 2
rs1550623 0.925 0.080 2 173348166 intron variant G/A snv 0.80 2