rs1557176576, 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 147921932 splice acceptor variant GG/TA mnv 0.700 0