Disease: Breast Carcinoma
Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11249433
EMBP1
0.827 0.160 1 121538815 intron variant A/C;G snv 3
rs11552449
AP4B1 ; DCLRE1B
0.925 0.080 1 113905767 missense variant C/G;T snv 0.22 0.15 2
rs4245739
MDM4
0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06 6
rs616488
PEX14
0.925 0.080 1 10506158 intron variant A/G snv 0.27 2
rs6678914
LGR6
0.882 0.080 1 202218048 intron variant G/A snv 0.37 2
rs12710696
LINC01376
0.925 0.080 2 19121042 intron variant T/A;C snv 2
rs13387042
LOC105373874 ; LOC101928278
0.732 0.280 2 217041109 intergenic variant A/G snv 0.44 3
rs13393577
ERBB4
0.851 0.120 2 212432139 intron variant T/C snv 0.10 2
rs1550623 0.925 0.080 2 173348166 intron variant G/A snv 0.80 2
rs16857609
DIRC3
0.925 0.080 2 217431785 intron variant C/T snv 0.28 2
rs2016394
DLX2-DT
0.925 0.080 2 172108243 intron variant G/A snv 0.40 2
rs4849887 0.807 0.080 2 120487546 intergenic variant T/A;C snv 3
rs12493607
TGFBR2
0.882 0.080 3 30641447 intron variant G/C;T snv 2
rs1357245
NEK10
0.925 0.080 3 27145111 intron variant C/T snv 0.35 2
rs4973768
SLC4A7
0.807 0.120 3 27374522 3 prime UTR variant C/T snv 0.44 2
rs6762644
ITPR1
0.925 0.080 3 4700592 intron variant A/G snv 0.38 2
rs6788895
SIAH2
0.882 0.080 3 150750021 intron variant G/T snv 0.18 2
rs17435444
TNIP3
0.925 0.080 4 121200339 intron variant A/G snv 4.8E-02 2
rs6828523
ADAM29
0.851 0.080 4 174925275 intron variant C/A snv 0.20 2
rs9790517
TET2
0.925 0.080 4 105163621 intron variant C/T snv 0.20 2
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 19
rs10472076 0.925 0.080 5 58888234 regulatory region variant T/A;C snv 2
rs10941679 0.763 0.120 5 44706396 intergenic variant A/G snv 0.25 2
rs1353747
PDE4D
0.882 0.080 5 59041654 intron variant T/G snv 6.9E-02 3
rs1432679
EBF1
0.851 0.080 5 158817075 intron variant C/T snv 0.44 2