Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11571747
BRCA2
1.000 0.080 13 32371035 missense variant A/C snv 1.1E-03 1.5E-03 1
rs397508869
BRCA1
1.000 0.080 17 43094138 missense variant A/C snv 1
rs56087561
BRCA2
1.000 0.080 13 32339425 missense variant A/C snv 2.2E-04 2.2E-04 1
rs28897675
BRCA1
1.000 0.080 17 43094795 missense variant A/C;G snv 3.1E-04 2.6E-04 1
rs28897687
BRCA1
1.000 0.080 17 43091823 missense variant A/C;G snv 2.6E-04 3.1E-04 1
rs397507838
BRCA2
1.000 0.080 13 32340636 missense variant A/C;G snv 8.2E-06 7.0E-06 1
rs397507847
BRCA2
1.000 0.080 13 32340739 missense variant A/C;G snv 1
rs397508994
BRCA1
0.925 0.080 17 43092856 stop gained A/C;G snv 1
rs587782190
BRCA1
0.882 0.200 17 43091731 stop gained A/C;G snv 7.0E-06 1
rs780723017
MANEA
1.000 0.080 6 95606008 missense variant A/C;G snv 4.0E-06 1
rs80356959
BRCA1
0.851 0.200 17 43045761 missense variant A/C;G snv 1
rs80357061
BRCA1
0.882 0.200 17 43067616 missense variant A/C;G snv 1
rs80357064
BRCA1
0.882 0.200 17 43106478 stop lost A/C;G snv 1.2E-05 1
rs80357474
BRCA1
0.827 0.200 17 43049188 missense variant A/C;G;T snv 8.0E-06 3
rs28897672
BRCA1
0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 2
rs45553935
BRCA1
0.851 0.200 17 43057122 missense variant A/C;G;T snv 2
rs1057519927
PIK3CA
0.716 0.240 3 179218295 missense variant A/C;G;T snv 1
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 1
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 1
rs17217772
MSH2
0.790 0.240 2 47410107 missense variant A/C;G;T snv 5.8E-03 1
rs397517201
PIK3CA
0.732 0.240 3 179218307 missense variant A/C;G;T snv 1
rs41293513
BRCA2
0.882 0.200 13 32363370 missense variant A/C;G;T snv 4.0E-06 1
rs80356929
BRCA1 ; NBR2
0.925 0.080 17 43124044 missense variant A/C;G;T snv 1
rs80357492
BRCA1
1.000 0.080 17 43082541 missense variant A/C;G;T snv 4.0E-06 1
rs41293463
BRCA1
0.790 0.280 17 43051071 missense variant A/C;T snv 1.2E-05 1