Source: CLINVAR ×
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: rs121912655
rs121912655
TP53
15 0.724 0.400 17 7674238 missense variant C/A;G;T snv 0.700 0
dbSNP: rs121912658
rs121912658
TP53
2 0.925 0.200 17 7676011 stop gained T/A;C;G snv 0.700 0
dbSNP: rs28934574
rs28934574
TP53
27 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 0.700 0
dbSNP: rs28934575
rs28934575
TP53
25 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.700 0
dbSNP: rs730882018
rs730882018
TP53
5 0.851 0.320 17 7676153 frameshift variant G/-;GG delins 0.700 0