Disease: Breast Carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1353747
PDE4D
0.882 0.080 5 59041654 intron variant T/G snv 6.9E-02 3
rs2380205 0.882 0.080 10 5844771 upstream gene variant C/T snv 0.47 3
rs56118985
INSL6 ; JAK2
0.882 0.080 9 5044432 missense variant G/A;C snv 1.8E-03; 4.0E-06 3
rs4971059
TRIM46
0.851 0.200 1 155176305 intron variant G/A snv 0.34 4
rs2296135
IL15RA
0.851 0.080 10 5952731 3 prime UTR variant A/C snv 0.58 5
rs762613037
SLC19A1 ; COL18A1
0.790 0.160 21 45512196 missense variant A/G snv 2.1E-05 7.0E-06 7
rs13347
CD44
0.763 0.320 11 35231725 3 prime UTR variant C/A;T snv 12
rs2228014
CXCR4
0.752 0.240 2 136115514 synonymous variant G/A snv 4.6E-02 3.5E-02 14
rs559063155
SF3B1
0.732 0.280 2 197402110 stop gained T/A;C;G snv 9.0E-05 14
rs1239681664
ABCA1
0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 15
rs371074389
LOC112268426 ; CXCR4
0.732 0.320 2 136115226 synonymous variant C/T snv 4.0E-06 4.2E-05 16
rs766914563
LOC112268426 ; CXCR4
0.732 0.320 2 136115082 synonymous variant C/T snv 7.0E-06 16
rs781172058
CXCR4
0.732 0.320 2 136115340 synonymous variant C/T snv 4.0E-06 16
rs1799930
NAT2
0.716 0.400 8 18400593 missense variant G/A snv 0.27 0.27 17
rs2735383
OSGIN2 ; NBN
0.708 0.360 8 89935041 3 prime UTR variant C/G snv 0.31 18
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs4553808
CTLA4
0.672 0.320 2 203866282 upstream gene variant A/G;T snv 0.16 28
rs1042028
SULT1A1
0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs2234767
FAS ; ACTA2
0.649 0.280 10 88989499 intron variant G/A;T snv 0.15 30
rs3745274
CYP2B6
0.672 0.480 19 41006936 missense variant G/A;T snv 4.0E-06; 0.27 30
rs763110
FASLG
0.653 0.560 1 172658358 upstream gene variant C/T snv 0.49 30
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs9282861
SULT1A1
0.658 0.440 16 28606193 missense variant C/T snv 31
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs886039484
TP53
0.641 0.440 17 7674888 missense variant T/C;G snv 32