Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28933370
MIR4728 ; ERBB2
0.882 0.120 17 39725125 missense variant A/G snv 7.0E-06 3
rs873330
LOC107984606
0.882 0.120 13 104807897 intergenic variant A/G snv 0.31 3
rs876658943
BRCA2
0.882 0.120 13 32332593 missense variant A/G snv 4.0E-06 3
rs9303542
SKAP1
0.882 0.120 17 48334138 intron variant A/G snv 0.34 3
rs273900729
BRCA1
0.925 0.160 17 43082529 missense variant A/G snv 2
rs12379183
BNC2
1.000 0.120 9 16865701 intron variant A/G snv 0.26 1
rs12451939
MED13
1.000 0.120 17 61970281 intron variant A/G snv 2.6E-02 1
rs121913279
PIK3CA
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs5275
PTGS2
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs1136201
ERBB2
0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs156697
GSTO2
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35 25
rs1801200
ERBB2
0.790 0.200 17 39723335 missense variant A/G;T snv 7
rs1256030
ESR2
0.827 0.240 14 64280452 intron variant A/G;T snv 6
rs2424932
DNMT3B
0.827 0.200 20 32808730 3 prime UTR variant A/G;T snv 5
rs80357438
NBR2 ; BRCA1
0.851 0.200 17 43124032 stop gained A/G;T snv 5
rs759920
DNMT1
0.882 0.120 19 10174102 intron variant A/G;T snv 3
rs80356993
BRCA1
0.925 0.120 17 43063937 missense variant A/G;T snv 3
rs12937080
BRIP1
1.000 0.120 17 61852376 intron variant A/G;T snv 1
rs7861573
BNC2
1.000 0.120 9 16862282 intron variant A/G;T snv 1
rs11571833
BRCA2
0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs6785617 0.882 0.120 3 172501054 downstream gene variant A/T snv 3.7E-02 4
rs608995
PGR
0.882 0.120 11 101035002 3 prime UTR variant A/T snv 0.27 3
rs80359477
BRCA2
0.851 0.200 13 32339386 frameshift variant AA/-;A delins 5
rs587781803
BRCA2
0.851 0.200 13 32341169 frameshift variant AAGAG/- delins 5
rs63750695
PMS2
0.851 0.280 7 5978675 frameshift variant AAGTT/- delins 6