Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1060502426
BRCA2
0.925 0.200 13 32338628 frameshift variant G/- del 2
rs1060502433
BRCA2
0.925 0.200 13 32357846 stop gained G/A;T snv 3
rs1060502437
BRCA2
0.925 0.200 13 32336827 frameshift variant A/- delins 2
rs1060502443
BRCA2
1.000 0.200 13 32394716 missense variant A/G snv 1
rs1060502444
BRCA2
0.925 0.200 13 32340428 frameshift variant TC/- delins 2
rs1060502449
BRCA2
0.925 0.200 13 32337461 stop gained G/A;T snv 3
rs1060502454
BRCA2
0.925 0.200 13 32332437 frameshift variant T/- del 3
rs1060502455
BRCA2
0.925 0.200 13 32336337 frameshift variant G/- del 2
rs1060502465
BRCA2
0.925 0.200 13 32326504 frameshift variant T/- del 2
rs1060502471
BRCA2
0.925 0.200 13 32371074 frameshift variant T/- delins 3
rs1060502475
BRCA2
0.925 0.200 13 32337431 frameshift variant A/- delins 2
rs1060502478
BRCA2
0.925 0.200 13 32362536 frameshift variant A/- del 3
rs1060502482
BRCA2
0.925 0.200 13 32356438 frameshift variant A/- delins 2
rs1060502484
BRCA2
0.925 0.200 13 32336587 frameshift variant A/- delins 3
rs1060502485
BRCA2
1.000 0.200 13 32326100 splice acceptor variant G/A snv 1
rs1060502601
RAD51C
0.882 0.200 17 58709884 frameshift variant T/- delins 4
rs1060505048
BRCA1
0.925 0.200 17 43045736 frameshift variant T/- del 3
rs1064792958
BRCA1
0.925 0.200 17 43094724 frameshift variant CAAGTTTGAAAC/T delins 2
rs1064792960
BRCA2
0.925 0.200 13 32319211 frameshift variant AACCATCTTATAATCA/- delins 2
rs1064792961
BRCA2
0.925 0.200 13 32337833 stop gained AGAG/TGAGGA delins 2
rs1064792962
BRCA2
0.925 0.200 13 32354968 frameshift variant CAAGCA/GC delins 2
rs1064793054
BRCA1
1.000 0.200 17 43104172 stop gained TGT/AGA mnv 2
rs1064793577
BRCA1
0.925 0.200 17 43076580 frameshift variant A/- del 3
rs1064793945
BRCA2
0.925 0.200 13 32332855 frameshift variant A/- delins 2
rs1064794018
BRCA2
1.000 0.200 13 32332968 stop gained C/G;T snv 2