rs186166891, SUGCT

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.
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 7 40367277 intron variant A/C;G;T snv 0.700 1.000 1 2016 2016