Source: BEFREE

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: rs863224683
rs863224683
TP53
17 7675224 missense variant G/A;C snv
CUI: C0007867
Disease: Cervix Diseases
Cervix Diseases 		0.010 1.000 1 2017 2017
dbSNP: rs863224683
rs863224683
TP53
17 7675224 missense variant G/A;C snv
CUI: C0007097
Disease: Carcinoma
Carcinoma 		0.010 1.000 1 2013 2013
dbSNP: rs863224683
rs863224683
TP53
17 7675224 missense variant G/A;C snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.010 1.000 1 2013 2013
dbSNP: rs863224683
rs863224683
TP53
17 7675224 missense variant G/A;C snv
CUI: C0333875
Disease: High-Grade Squamous Intraepithelial Lesions
High-Grade Squamous Intraepithelial Lesions 		0.010 1.000 1 2017 2017