rs3754701, RAMP1

N. diseases: 4
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.
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.882 0.120 2 237858561 upstream gene variant A/C;T snv 0.010 1.000 1 2010 2010
Common Migraine
CUI: C0338480
Disease: Common Migraine
62 0.882 0.120 2 237858561 upstream gene variant A/C;T snv 0.010 1.000 1 2015 2015
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.882 0.120 2 237858561 upstream gene variant A/C;T snv 0.010 1.000 1 2017 2017
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.882 0.120 2 237858561 upstream gene variant A/C;T snv 0.010 1 2013 2013