rs1358919643, FGFR2

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.
Pfeiffer Syndrome
CUI: C0220658
Disease: Pfeiffer Syndrome
36 1.000 0.080 10 121517463 missense variant C/A;T snv 4.0E-06 0.700 1.000 2 1995 1998