Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6503691
rs6503691
STAT5B
0.827 0.200 17 42242072 intron variant C/T snv 0.26
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.020 1.000 2 2007 2015
dbSNP: rs6503691
rs6503691
STAT5B
0.827 0.200 17 42242072 intron variant C/T snv 0.26
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.020 1.000 2 2007 2015
dbSNP: rs6503691
rs6503691
STAT5B
0.827 0.200 17 42242072 intron variant C/T snv 0.26
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
Myeloid Leukemia, Chronic 		0.010 1.000 1 2010 2010
dbSNP: rs6503691
rs6503691
STAT5B
0.827 0.200 17 42242072 intron variant C/T snv 0.26
CUI: C0035439
Disease: Rheumatic Heart Disease
Rheumatic Heart Disease 		0.010 1.000 1 2014 2014
dbSNP: rs6503691
rs6503691
STAT5B
0.827 0.200 17 42242072 intron variant C/T snv 0.26
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic 		0.010 1.000 1 2012 2012