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: rs786202962
rs786202962
TP53
0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		0.010 1.000 1 2004 2004
dbSNP: rs786202962
rs786202962
TP53
0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		0.010 1.000 1 2004 2004
dbSNP: rs786202962
rs786202962
TP53
0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.010 1.000 1 2004 2004
dbSNP: rs786202962
rs786202962
TP53
0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2015 2015