Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs765848205
rs765848205
TP53
12 0.763 0.240 17 7674253 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs786203436
rs786203436
TP53
20 0.701 0.280 17 7675125 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs864622237
rs864622237
TP53
17 0.716 0.320 17 7674263 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs876659675
rs876659675
TP53
8 0.807 0.280 17 7674199 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs876660333
rs876660333
TP53
13 0.742 0.360 17 7673805 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs876660821
rs876660821
TP53
22 0.689 0.400 17 7675075 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs967461896
rs967461896
TP53
17 0.724 0.240 17 7675086 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs28897672
rs28897672
BRCA1
16 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 0.700 0
dbSNP: rs397509173
rs397509173
BRCA1
4 0.925 0.200 17 43104120 splice donor variant A/C;G;T snv 0.700 0
dbSNP: rs80357006
rs80357006
BRCA1
4 0.925 0.200 17 43092274 stop gained A/C;G;T snv 1.2E-05 0.700 0
dbSNP: rs1057519938
rs1057519938
PIK3CA
10 0.776 0.160 3 179203764 missense variant A/C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1057520004
rs1057520004
TP53
12 0.752 0.240 17 7674884 missense variant A/C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs121913476
rs121913476
FGFR2
7 0.851 0.080 10 121498520 missense variant A/C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs2273535
rs2273535
AURKA
38 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 0.010 1.000 1 2014 2014
dbSNP: rs41293463
rs41293463
BRCA1
9 0.790 0.280 17 43051071 missense variant A/C;T snv 1.2E-05 0.010 1.000 1 1999 1999
dbSNP: rs587781632
rs587781632
BRCA1
4 0.925 0.200 17 43106476 splice donor variant A/C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs6505162
rs6505162
NSRP1 ; MIR423 ; MIR3184
25 0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 0.010 1.000 1 2018 2018
dbSNP: rs7716600
rs7716600 		4 0.925 0.080 5 44874903 regulatory region variant A/C;T snv 0.010 1.000 1 2014 2014
dbSNP: rs796065354
rs796065354
ESR1
9 0.882 0.080 6 151944320 missense variant A/G snv 0.040 1.000 4 2005 2009
dbSNP: rs1462893414
rs1462893414
ESR1
5 0.882 0.080 6 151944323 missense variant A/G snv 4.0E-06 7.0E-06 0.030 1.000 3 2005 2007
dbSNP: rs1057519727
rs1057519727
HERC2
1 15 28260829 missense variant A/G snv 0.700 1.000 1 2013 2013
dbSNP: rs1057519914
rs1057519914
MTOR
5 0.851 0.240 1 11157174 missense variant A/G snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519933
rs1057519933
PIK3CA
11 0.790 0.240 3 179199156 missense variant A/G snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519935
rs1057519935
PIK3CA
11 0.790 0.240 3 179199157 missense variant A/G snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519960
rs1057519960
SF3B2
7 0.827 0.280 11 66063413 missense variant A/G snv 0.700 1.000 1 2016 2016