rs7926987, FOLR3

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.
Meningomyelocele
CUI: C0025312
Disease: Meningomyelocele
27 1.000 0.080 11 72138457 intron variant C/G;T snv 0.010 1.000 1 2010 2010