Disease: Breast Carcinoma
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
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
rs11249433
EMBP1
0.827 0.160 1 121538815 intron variant A/C;G snv 3
rs11780156
PVT1
0.925 0.080 8 128182395 intron variant C/T snv 0.13 2
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 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
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
rs13281615
CASC8 ; POU5F1B ; PCAT1 ; CASC21
0.716 0.360 8 127343372 intron variant A/G snv 0.43 3
rs13329835
CDYL2
0.925 0.080 16 80616908 intron variant A/G snv 0.35 2
rs13393577
ERBB4
0.851 0.120 2 212432139 intron variant T/C snv 0.10 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
rs1562430
PCAT1 ; CASC8 ; CASC21 ; POU5F1B
0.807 0.160 8 127375606 intron variant T/C snv 0.41 2
rs16857609
DIRC3
0.925 0.080 2 217431785 intron variant C/T snv 0.28 2
rs17356907
PGAM1P5
0.925 0.080 12 95633983 intron variant A/G snv 0.28 3
rs17435444
TNIP3
0.925 0.080 4 121200339 intron variant A/G snv 4.8E-02 2