Disease: Breast Carcinoma
Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587782471
CHEK2
0.851 0.240 22 28711994 missense variant A/G;T snv 3.5E-04; 8.0E-06 4
rs10771399 0.827 0.080 12 28002147 intergenic variant A/G snv 8.9E-02 3
rs10995190
ZNF365
0.882 0.080 10 62518923 intron variant G/A snv 0.16 3
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
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
rs13281615
CASC8 ; POU5F1B ; PCAT1 ; CASC21
0.716 0.360 8 127343372 intron variant A/G snv 0.43 3
rs13387042
LOC105373874 ; LOC101928278
0.732 0.280 2 217041109 intergenic variant A/G snv 0.44 3
rs1353747
PDE4D
0.882 0.080 5 59041654 intron variant T/G snv 6.9E-02 3
rs16886165 0.882 0.160 5 56727256 intergenic variant T/C;G snv 0.22 3
rs17356907
PGAM1P5
0.925 0.080 12 95633983 intron variant A/G snv 0.28 3
rs1978503
LINC01416 ; LOC107985164
0.882 0.160 18 55997051 non coding transcript exon variant A/G snv 0.18 3
rs2075555
COL1A1
0.807 0.240 17 50196930 intron variant T/A;G snv 3
rs2180341
RNF146
0.882 0.160 6 127279485 intron variant G/A snv 0.73 3
rs2284378
RALY
0.851 0.080 20 34000289 intron variant T/C;G snv 3
rs2380205 0.882 0.080 10 5844771 upstream gene variant C/T snv 0.47 3
rs2981582
FGFR2
0.695 0.360 10 121592803 intron variant A/G snv 0.58 3
rs3803662
CASC16
0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 3
rs3817198
LSP1
0.790 0.280 11 1887776 intron variant T/C snv 0.26 3
rs4849887 0.807 0.080 2 120487546 intergenic variant T/A;C snv 3
rs6556756
LOC105377703 ; LINC02143
0.882 0.160 5 164462274 intron variant G/T snv 0.89 3
rs7072776
MLLT10 ; LOC107984214
0.925 0.080 10 21744013 downstream gene variant A/G snv 0.65 3
rs7107217 0.882 0.160 11 129603795 intron variant A/C;G snv 3
rs777741666
ATM ; C11orf65
0.925 0.080 11 108327759 splice donor variant G/A;T snv 3