Disease: Malignant neoplasm of breast
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10146997
NRXN3
0.827 0.240 14 79478819 intron variant A/G snv 0.25 6
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs1271572
ESR2
0.708 0.400 14 64295199 intron variant A/C;T snv 16
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs1477196
FTO
0.851 0.200 16 53774346 intron variant A/G snv 0.71 7
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs7713645
PIK3R1
0.851 0.200 5 68231498 intron variant A/C snv 0.58 4
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
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
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs13188458 0.882 0.160 5 8127718 intergenic variant T/G snv 0.22 4
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs7566605
LOC107985940
0.752 0.320 2 118078449 regulatory region variant C/G snv 0.70 11
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs5744168
TLR5
0.701 0.480 1 223111858 stop gained G/A snv 5.3E-02 4.4E-02 18
rs1042028
SULT1A1
0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63