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: C0700095
Disease: Central neuroblastoma
Central 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
Conventional (Clear Cell) 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
Squamous cell carcinoma of the head and neck
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: 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
dbSNP: rs2273535
rs2273535
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.020 1.000 2 2007 2009
dbSNP: rs2273535
rs2273535
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.020 1.000 2 2016 2018
dbSNP: rs2273535
rs2273535
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28
Malignant neoplasm of colon and/or rectum
0.020 0.500 2 2006 2014
dbSNP: rs2273535
rs2273535
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28
CUI: C0009375
Disease: Colonic Neoplasms
Colonic Neoplasms
0.020 1.000 2 2003 2005
dbSNP: rs2273535
rs2273535
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma
0.020 1.000 2 2015 2019
dbSNP: rs2273535
rs2273535
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.020 1.000 2 2016 2018
dbSNP: rs2273535
rs2273535
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.020 0.500 2 2006 2014
dbSNP: rs2273535
rs2273535
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.020 1.000 2 2007 2009
dbSNP: rs2273535
rs2273535
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.020 1.000 2 2017 2018
dbSNP: rs2273535
rs2273535
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.020 1.000 2 2018 2018