rs1801516, ATM

N. diseases: 39
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 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.100 0.786 14 2003 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.100 0.786 14 2003 2019
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2019 2019
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2019 2019
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2019 2019
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.070 0.714 7 2005 2018
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.060 0.667 6 2005 2018
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2018 2018
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2018 2018
Plexiform leiomyoma
CUI: C2242776
Disease: Plexiform leiomyoma
103 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.700 1.000 1 2018 2018
Uterine Fibroids
CUI: C0042133
Disease: Uterine Fibroids
154 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.700 1.000 1 2018 2018
melanoma
CUI: C0025202
Disease: melanoma
515 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.810 1.000 3 2011 2017
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.030 1.000 3 2009 2016
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1 2016 2016
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2016 2016
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2016 2016
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.020 1.000 2 2011 2015
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2015 2015
Differentiated Thyroid Gland Carcinoma
CUI: C1337013
Disease: Differentiated Thyroid Gland Carcinoma
80 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1 2015 2015
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
315 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2015 2015
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2015 2015
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2014 2014
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2014 2014
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2012 2012
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2012 2012