rs1566734, PTPRJ

N. diseases: 10
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.
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.807 0.120 11 48123823 missense variant A/C snv 0.17 0.15 0.730 0.667 3 2005 2019
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.807 0.120 11 48123823 missense variant A/C snv 0.17 0.15 0.700 0
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.807 0.120 11 48123823 missense variant A/C snv 0.17 0.15 0.030 0.333 3 2008 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.807 0.120 11 48123823 missense variant A/C snv 0.17 0.15 0.030 0.333 3 2008 2019
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.807 0.120 11 48123823 missense variant A/C snv 0.17 0.15 0.020 0.500 2 2008 2019
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.807 0.120 11 48123823 missense variant A/C snv 0.17 0.15 0.010 1.000 1 2008 2008
Malignant neoplasm of thyroid
CUI: C0007115
Disease: Malignant neoplasm of thyroid
103 0.807 0.120 11 48123823 missense variant A/C snv 0.17 0.15 0.010 1.000 1 2004 2004
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.807 0.120 11 48123823 missense variant A/C snv 0.17 0.15 0.010 1.000 1 2004 2004
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.807 0.120 11 48123823 missense variant A/C snv 0.17 0.15 0.010 1.000 1 2010 2010
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.807 0.120 11 48123823 missense variant A/C snv 0.17 0.15 0.010 1.000 1 2004 2004