rs1093538, FAM189A1

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.
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 1.000 0.040 15 29326124 intron variant C/T snv 0.12 0.010 1.000 1 2018 2018
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 1.000 0.040 15 29326124 intron variant C/T snv 0.12 0.010 1.000 1 2018 2018