rs1136201, ERBB2

N. diseases: 34
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.100 0.895 38 2000 2018
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.100 0.895 38 2000 2018
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.020 0.500 2 2002 2019
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.020 0.500 2 2002 2019
Benign Prostatic Hyperplasia
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
91 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2004 2004
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2004 2004
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2004 2004
Breast Cancer, Familial
CUI: C0346153
Disease: Breast Cancer, Familial
91 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2005 2005
Invasive carcinoma of breast
CUI: C0853879
Disease: Invasive carcinoma of breast
21 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2005 2005
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.050 0.600 5 2007 2013
Fibroadenoma
CUI: C0206650
Disease: Fibroadenoma
1 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2008 2008
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1 2008 2008
Secondary Neoplasm
CUI: C2939419
Disease: Secondary Neoplasm
85 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1 2008 2008
Malignant neoplasm of thyroid
CUI: C0007115
Disease: Malignant neoplasm of thyroid
103 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2009 2009
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2009 2009
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2009 2009
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.030 0.667 3 2010 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.030 0.667 3 2010 2019
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2010 2010
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2010 2010
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2010 2010
HER2-positive carcinoma of breast
CUI: C1960398
Disease: HER2-positive carcinoma of breast
26 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.020 1.000 2 2014 2015
HER2-negative breast cancer
CUI: C4733095
Disease: HER2-negative breast cancer
18 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1 2014 2014
Childhood Osteosarcoma
CUI: C1332986
Disease: Childhood Osteosarcoma
151 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2015 2015
Malignant neoplasm of gallbladder
CUI: C0153452
Disease: Malignant neoplasm of gallbladder
81 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2015 2015