Disease: Breast Carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 22
rs1057520006
TP53
0.752 0.240 17 7673799 missense variant A/C;G;T snv 14
rs1057520036
FGFR4
0.925 0.080 5 177093180 missense variant A/G snv 3
rs10941679 0.763 0.120 5 44706396 intergenic variant A/G snv 0.25 11
rs11249433
EMBP1
0.827 0.160 1 121538815 intron variant A/C;G snv 9
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs11895168
ERBB4
0.925 0.080 2 211377467 3 prime UTR variant A/C snv 0.68 4
rs121913273
PIK3CA
0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs121913470
ERBB2
0.776 0.200 17 39723967 missense variant T/C;G snv 13
rs121913471
MIR4728 ; ERBB2
0.807 0.120 17 39724747 missense variant G/A;C;T snv 8
rs1239905891
IGF1
0.925 0.080 12 102475786 missense variant G/A;T snv 3
rs13283662
UHRF2
0.925 0.080 9 6428530 intron variant T/C snv 4
rs17506395
TP63
0.925 0.080 3 189803530 intron variant T/G snv 0.19 3
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 22
rs1972820
ERBB4
0.925 0.080 2 211378697 3 prime UTR variant G/A snv 0.63 3
rs2787486
STXBP4
0.925 0.080 17 55132413 intron variant A/C snv 0.33 3
rs375874539
TP53
0.732 0.320 17 7674237 missense variant G/A;C snv 15
rs3803662
CASC16
0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4784227
CASC16
0.807 0.160 16 52565276 intron variant C/T snv 0.20 8
rs587777790
PIK3CA
0.732 0.280 3 179199690 missense variant G/A snv 14
rs587780071
TP53
0.732 0.240 17 7674951 missense variant G/A snv 15
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs7716600 0.925 0.080 5 44874903 regulatory region variant A/C;T snv 4