Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs573154688
rs573154688
TP53
1.000 0.160 17 7670711 missense variant C/T snv 4.4E-05 3.5E-05
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.010 1.000 1 2018 2018
dbSNP: rs573154688
rs573154688
TP53
1.000 0.160 17 7670711 missense variant C/T snv 4.4E-05 3.5E-05
CUI: C0406704
Disease: Rudiger syndrome 1
Rudiger syndrome 1 		0.010 1.000 1 2012 2012
dbSNP: rs573154688
rs573154688
TP53
1.000 0.160 17 7670711 missense variant C/T snv 4.4E-05 3.5E-05
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 < 0.001 1 2010 2010