rs6503691, STAT5B

N. diseases: 5
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 0.827 0.200 17 42242072 intron variant C/T snv 0.26 0.020 1.000 2 2007 2015
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.827 0.200 17 42242072 intron variant C/T snv 0.26 0.020 1.000 2 2007 2015
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.827 0.200 17 42242072 intron variant C/T snv 0.26 0.010 1.000 1 2012 2012
Myeloid Leukemia, Chronic
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
115 0.827 0.200 17 42242072 intron variant C/T snv 0.26 0.010 1.000 1 2010 2010
Rheumatic Heart Disease
CUI: C0035439
Disease: Rheumatic Heart Disease
33 0.827 0.200 17 42242072 intron variant C/T snv 0.26 0.010 1.000 1 2014 2014