rs653747, LINC00923

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 15 97659878 intron variant C/T snv 0.48 0.010 1.000 1 2017 2017
Kidney Diseases
CUI: C0022658
Disease: Kidney Diseases
140 15 97659878 intron variant C/T snv 0.48 0.010 1.000 1 2017 2017