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: rs587782329
rs587782329
TP53
23 0.677 0.280 17 7674217 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
dbSNP: rs730882025
rs730882025
TP53
21 0.724 0.360 17 7674885 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
dbSNP: rs863224683
rs863224683
TP53
4 17 7675224 missense variant G/A;C snv 0.010 1.000 1 2017 2017