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: rs2273535
rs2273535
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial
0.010 1.000 1 2004 2004
dbSNP: rs2273535
rs2273535
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28
CUI: C1140680
Disease: Malignant neoplasm of ovary
Malignant neoplasm of ovary
0.010 1.000 1 2004 2004
dbSNP: rs2273535
rs2273535
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28
Squamous cell carcinoma of esophagus
0.010 1.000 1 2004 2004
dbSNP: rs2273535
rs2273535
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28
CUI: C0521158
Disease: Recurrent tumor
Recurrent tumor
0.010 1.000 1 2012 2012
dbSNP: rs2273535
rs2273535
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma
0.010 1.000 1 2018 2018
dbSNP: rs2273535
rs2273535
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm
0.010 1.000 1 2004 2004
dbSNP: rs2273535
rs2273535
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28
CUI: C0153567
Disease: Uterine Cancer
Uterine Cancer
0.010 1.000 1 2007 2007
dbSNP: rs2273535
rs2273535
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2007 2007
dbSNP: rs2273535
rs2273535
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.010 1.000 1 2014 2014
dbSNP: rs2273535
rs2273535
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
0.010 < 0.001 1 2007 2007
dbSNP: rs2273535
rs2273535
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28
CUI: C4086165
Disease: Childhood Neuroblastoma
Childhood Neuroblastoma
0.010 1.000 1 2018 2018
dbSNP: rs2273535
rs2273535
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28
CUI: C1134719
Disease: Invasive Ductal Breast Carcinoma
Invasive Ductal Breast Carcinoma
0.010 1.000 1 2017 2017