Disease: Malignant neoplasm of breast
Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1003623
ATM
0.925 0.080 11 108281855 intron variant C/G;T snv 2
rs10053538
HAVCR2
0.807 0.160 5 157110499 intron variant C/A;T snv 7
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 40
rs10077427
POLK
0.925 0.080 5 75542076 intron variant A/G snv 0.13 2
rs1008805
MIR4713HG ; CYP19A1
0.851 0.160 15 51257402 intron variant G/A snv 0.64 7
rs10109984
PRKDC
0.925 0.080 8 47891114 intron variant T/C snv 0.54 4
rs1011970
CDKN2B-AS1
0.677 0.320 9 22062135 intron variant G/T snv 0.23 6
rs1012477
PER3
0.827 0.160 1 7798075 intron variant G/C snv 0.16 8
rs10145182
NIN
0.925 0.080 14 50809291 intron variant T/A;C;G snv 2
rs10146997
NRXN3
0.827 0.240 14 79478819 intron variant A/G snv 0.25 4
rs10165970
NPAS2
0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs1017226
MAP3K1
0.925 0.080 5 56857565 intron variant T/C snv 5.8E-02 2
rs10175338
CYP1B1-AS1 ; CYP1B1
0.925 0.080 2 38080501 intron variant G/T snv 0.25 2
rs10235235
ZNF394 ; ZNF789
0.925 0.080 7 99478208 intron variant T/C snv 0.13 3
rs10273424
TMEM225B
0.925 0.080 7 99598450 intron variant T/A snv 0.13 2
rs1029946
PRKAG2
0.925 0.080 7 151578720 intron variant A/G snv 0.21 2
rs1033662
LINC01524 ; LOC105372666
0.925 0.080 20 52408842 intron variant A/G snv 0.46 2
rs1038304
CCDC170 ; LOC107986528
0.882 0.160 6 151612040 intron variant A/G snv 0.58 3
rs10439478
ACYP2
0.925 0.080 2 54232313 intron variant A/C;G;T snv 2
rs10463297
SRA1
0.925 0.080 5 140556654 intron variant T/C snv 0.29 2
rs10474352
ARRDC3-AS1
0.925 0.080 5 91436408 intron variant C/T snv 0.23 2
rs10477313
PPP2R2B
0.925 0.080 5 146854076 intron variant C/T snv 0.17 2
rs10483028
RUNX1
0.925 0.080 21 35301275 intron variant C/T snv 0.18 2
rs10483813
RAD51B
0.851 0.120 14 68564567 intron variant T/A;C snv 4
rs10485805
AURKA
0.925 0.080 20 56370727 intron variant A/G snv 0.23 2