rs182830086, FMR1

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.
Fragile X Syndrome
CUI: C0016667
Disease: Fragile X Syndrome
11 1.000 0.080 X 147944892 missense variant G/T snv 5.5E-06 0.010 1.000 1 2012 2012