Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs80357327
BRCA1
0.827 0.200 17 43115730 missense variant A/C;G;T snv 6
rs80357440
BRCA1
0.827 0.200 17 43091638 stop gained G/A;C;T snv 4.0E-06 6
rs80357446
BRCA1
0.827 0.200 17 43115729 missense variant C/A;T snv 6
rs80357475
BRCA1 ; NBR2
0.827 0.200 17 43124094 start lost C/A;G;T snv 6
rs80358079
BRCA1
0.827 0.200 17 43057147 intron variant C/T snv 6
rs80358189
BRCA1
0.827 0.200 17 43074522 splice acceptor variant C/A;G;T snv 1.2E-05 6
rs886040898
BRCA1
0.827 0.200 17 43115743 stop gained A/C;T snv 6
rs1800747
BRCA1
0.882 0.200 17 43063952 splice acceptor variant C/A;G;T snv 5
rs1800751
BRCA1
0.851 0.160 17 43047676 missense variant G/A;C snv 4.0E-06 5
rs273899698
BRCA1
0.851 0.080 17 43092434 stop gained C/A;T snv 5
rs397509205
BRCA1
0.882 0.080 17 43070984 stop gained C/A snv 5
rs786202998
BRCA1
0.851 0.080 17 43091030 stop gained C/A;T snv 5
rs80187739
BRCA1
0.851 0.200 17 43067608 missense variant C/A;G;T snv 1.2E-05 5
rs80356880
BRCA1
0.851 0.080 17 43115750 missense variant G/C;T snv 5
rs80356923
BRCA1
0.882 0.200 17 43091891 stop gained C/A;T snv 9.9E-05 5
rs80356932
BRCA1
0.851 0.200 17 43076600 stop gained G/A snv 5
rs80356936
BRCA1
0.851 0.200 17 43104260 stop gained A/C;G;T snv 4.0E-06 5
rs80356959
BRCA1
0.851 0.200 17 43045761 missense variant A/C;G snv 5
rs80357034
BRCA1
0.882 0.200 17 43067610 missense variant G/A;C;T snv 5
rs80357164
BRCA1
0.851 0.200 17 43115745 missense variant A/C;G;T snv 5
rs80357287
NBR2 ; BRCA1
0.882 0.200 17 43124096 start lost T/C snv 5
rs80357307
BRCA1
0.851 0.200 17 43045760 stop gained C/T snv 5
rs80357350
BRCA1
0.827 0.200 17 43104928 stop gained G/A;C snv 5
rs80357367
BRCA1
0.851 0.200 17 43057090 stop gained G/A snv 5
rs80357433
BRCA1
0.851 0.200 17 43071225 stop gained G/A;C snv 4.0E-06 1.4E-05 5