rs1800057, ATM

N. diseases: 11
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.
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.776 0.200 11 108272729 missense variant C/A;G snv 1.7E-02 0.730 0.750 4 2004 2018
Plexiform leiomyoma
CUI: C2242776
Disease: Plexiform leiomyoma
103 0.776 0.200 11 108272729 missense variant C/A;G snv 1.7E-02 0.700 1.000 1 2018 2018
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
288 0.776 0.200 11 108272729 missense variant C/A;G snv 1.7E-02 0.700 1.000 1 2017 2017
Uterine Fibroids
CUI: C0042133
Disease: Uterine Fibroids
154 0.776 0.200 11 108272729 missense variant C/A;G snv 1.7E-02 0.700 1.000 1 2018 2018
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.776 0.200 11 108272729 missense variant C/A;G snv 1.7E-02 0.040 1.000 4 2002 2018
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.776 0.200 11 108272729 missense variant C/A;G snv 1.7E-02 0.040 1.000 4 2002 2018
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.776 0.200 11 108272729 missense variant C/A;G snv 1.7E-02 0.030 0.667 3 2004 2009
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.776 0.200 11 108272729 missense variant C/A;G snv 1.7E-02 0.010 1.000 1 2006 2006
Differentiated Thyroid Gland Carcinoma
CUI: C1337013
Disease: Differentiated Thyroid Gland Carcinoma
80 0.776 0.200 11 108272729 missense variant C/A;G snv 1.7E-02 0.010 1.000 1 2012 2012
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.776 0.200 11 108272729 missense variant C/A;G snv 1.7E-02 0.010 1.000 1 2006 2006
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.776 0.200 11 108272729 missense variant C/A;G snv 1.7E-02 0.010 1.000 1 2006 2006