rs10199956, RAMP1

N. diseases: 1
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 2 237907946 intron variant T/A;G snv 0.010 1.000 1 2017 2017