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: rs587782329
rs587782329
TP53
0.677 0.280 17 7674217 missense variant C/A;G;T snv
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.020 1.000 2 2000 2004
dbSNP: rs587782329
rs587782329
TP53
0.677 0.280 17 7674217 missense variant C/A;G;T snv
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		0.020 1.000 2 2000 2004
dbSNP: rs587782329
rs587782329
TP53
0.677 0.280 17 7674217 missense variant C/A;G;T snv
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		0.020 1.000 2 2000 2004
dbSNP: rs587782329
rs587782329
TP53
0.677 0.280 17 7674217 missense variant C/A;G;T snv
CUI: C0024121
Disease: Lung Neoplasms
Lung Neoplasms 		0.010 1.000 1 1997 1997
dbSNP: rs587782329
rs587782329
TP53
0.677 0.280 17 7674217 missense variant C/A;G;T snv
CUI: C0851140
Disease: Carcinoma in situ of uterine cervix
Carcinoma in situ of uterine cervix 		0.010 1.000 1 2000 2000
dbSNP: rs587782329
rs587782329
TP53
0.677 0.280 17 7674217 missense variant C/A;G;T snv
CUI: C0007867
Disease: Cervix Diseases
Cervix Diseases 		0.010 1.000 1 2017 2017
dbSNP: rs587782329
rs587782329
TP53
0.677 0.280 17 7674217 missense variant C/A;G;T snv
CUI: C0333875
Disease: High-Grade Squamous Intraepithelial Lesions
High-Grade Squamous Intraepithelial Lesions 		0.010 1.000 1 2017 2017