Disease: Endometrial Carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12185157
CDH1
0.882 0.120 16 68750684 intron variant G/A;C;T snv 3
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 17
rs1271572
ESR2
0.708 0.400 14 64295199 intron variant A/C;T snv 16
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs17715799
CDH1
0.882 0.120 16 68796608 intron variant A/G;T snv 3
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs2699887
PIK3CA ; LOC101928739
0.763 0.280 3 179148620 intron variant C/T snv 0.18 11
rs28566535
CYP19A1
0.851 0.120 15 51308944 intron variant A/C;G;T snv 4
rs3020314
ESR1
0.790 0.280 6 151949537 intron variant C/G;T snv 7
rs3020449
ESR2
0.807 0.200 14 64306674 intron variant A/G;T snv 10
rs3737559
BRCA1
0.882 0.120 17 43082287 intron variant C/T snv 6.9E-02 3
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs4775936
MIR4713HG ; CYP19A1
0.790 0.200 15 51243825 intron variant C/T snv 0.36 7
rs6443624
PIK3CA
0.776 0.200 3 179179886 intron variant C/A snv 0.30 8
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs8175347
UGT1A9 ; UGT1A1 ; UGT1A6 ; UGT1A10 ; UGT1A8 ; UGT1A3 ; UGT1A5 ; UGT1A7 ; UGT1A4
0.708 0.400 2 233760234 intron variant TATA/-;TA;TATATA;TATATATA;TATATATATA;TATATATATATA delins 16
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 14
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs10012
CYP1B1 ; CYP1B1-AS1
0.716 0.280 2 38075247 missense variant G/C snv 0.31 0.36 16
rs1042028
SULT1A1
0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30