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: rs112431538
rs112431538
TP53
1.000 0.120 17 7673767 missense variant C/T snv 7.0E-06
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome 		0.700 1.000 9 1997 2015
dbSNP: rs112431538
rs112431538
TP53
1.000 0.120 17 7673767 missense variant C/T snv 7.0E-06
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		0.700 1.000 8 2000 2013
dbSNP: rs112431538
rs112431538
TP53
1.000 0.120 17 7673767 missense variant C/T snv 7.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2017 2017
dbSNP: rs112431538
rs112431538
TP53
1.000 0.120 17 7673767 missense variant C/T snv 7.0E-06
CUI: C0009375
Disease: Colonic Neoplasms
Colonic Neoplasms 		0.010 1.000 1 2017 2017