Disease: Breast Carcinoma
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
rs11249433
EMBP1
0.827 0.160 1 121538815 intron variant A/C;G snv 3
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
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
rs137853007
CHEK2
0.790 0.240 22 28725254 missense variant G/A;T snv 5.2E-05 8
rs1555616176
BRIP1
0.925 0.080 17 61849196 frameshift variant T/- del 2
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 7
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 15
rs2075555
COL1A1
0.807 0.240 17 50196930 intron variant T/A;G snv 3
rs2236007
LOC105370455 ; PAX9
0.925 0.080 14 36663564 intron variant G/A;C snv 0.18; 8.6E-06 2
rs2284378
RALY
0.851 0.080 20 34000289 intron variant T/C;G snv 3
rs28897672
BRCA1
0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 10
rs2912774
FGFR2
0.925 0.080 10 121589148 intron variant T/A;G snv 2
rs2981578
FGFR2
0.925 0.080 10 121580797 intron variant C/A;T snv 2
rs3750817
FGFR2
0.851 0.080 10 121573063 intron variant C/G;T snv 2
rs41293497
BRCA2
0.724 0.440 13 32340037 stop gained C/A;G;T snv 4.0E-06; 2.0E-05 14
rs4245739
MDM4
0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06 6
rs4849887 0.807 0.080 2 120487546 intergenic variant T/A;C snv 3
rs554219 0.925 0.080 11 69516874 regulatory region variant C/A;G;T snv 2
rs587782471
CHEK2
0.851 0.240 22 28711994 missense variant A/G;T snv 3.5E-04; 8.0E-06 4
rs7107217 0.882 0.160 11 129603795 intron variant A/C;G snv 3