rs10501367, APLNR

N. diseases: 2
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.
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 1.000 0.040 11 57238113 upstream gene variant T/C snv 0.73 0.040 1.000 4 2009 2018
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 1.000 0.040 11 57238113 upstream gene variant T/C snv 0.73 0.020 1.000 2 2010 2016