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: rs17849781
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms 		0.710 1.000 1 2014 2016
dbSNP: rs17849781
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.030 1.000 3 2017 2019
dbSNP: rs17849781
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.030 1.000 3 2017 2019
dbSNP: rs17849781
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.020 1.000 2 2004 2008
dbSNP: rs17849781
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.020 1.000 2 2004 2008
dbSNP: rs17849781
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.010 1.000 1 2019 2019
dbSNP: rs17849781
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv
CUI: C0149925
Disease: Small cell carcinoma of lung
Small cell carcinoma of lung 		0.010 1.000 1 1991 1991
dbSNP: rs17849781
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv
CUI: C0027765
Disease: nervous system disorder
nervous system disorder 		0.010 1.000 1 2019 2019