rs77543610, FGFR2

N. diseases: 28
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.
Ramer Ladda syndrome
CUI: C2930865
Disease: Ramer Ladda syndrome
2 0.667 0.560 10 121520160 missense variant G/C snv 0.010 1.000 1 2003 2003
Strabismus
CUI: C0038379
Disease: Strabismus
89 0.667 0.560 10 121520160 missense variant G/C snv 0.010 1.000 1 2006 2006
Superior rectus muscle underaction
CUI: C4703722
Disease: Superior rectus muscle underaction
1 0.667 0.560 10 121520160 missense variant G/C snv 0.010 1.000 1 2006 2006