Disease: Breast Carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs6214
LINC02456 ; HELLPAR ; IGF1
0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 26
rs11205303
MTMR11
0.882 0.120 1 149934520 missense variant T/C snv 0.33 0.29 9
rs45446698
CYP3A7-CYP3A51P ; CYP3A7 ; ZSCAN25
0.807 0.120 7 99735325 upstream gene variant T/G snv 2.7E-02 9
rs1966265
FGFR4
0.827 0.160 5 177089630 missense variant G/A;T snv 0.25 8
rs6024836
FAM210B ; AURKA
0.851 0.160 20 56369012 downstream gene variant G/A snv 0.42 7
rs6569648
L3MBTL3
1.000 0.080 6 130027974 intron variant C/T snv 0.84 7
rs572169
GHSR
0.882 0.160 3 172447937 synonymous variant C/T snv 0.31 0.24 6
rs592373
LSP1
0.925 0.080 11 1869760 intron variant G/A;T snv 0.63; 6.8E-06 5
rs7223535
ATAD5
1.000 0.080 17 30884649 intron variant G/A snv 0.25 4
rs1061651
TBX3
0.925 0.080 12 114670556 3 prime UTR variant T/C snv 3
rs12325489
LOC107983961 ; CASC22
0.925 0.080 16 52273164 non coding transcript exon variant C/T snv 0.27 3
rs3798758
ESR1
0.925 0.080 6 152100719 3 prime UTR variant C/A snv 7.4E-02 3
rs754532
SART1
0.925 0.080 11 65979586 3 prime UTR variant G/A;C snv 3
rs310291 1.000 0.080 8 23801998 downstream gene variant G/A;C snv 2
rs3853291 1.000 0.080 11 44347927 intergenic variant G/A;C snv 2