rs121918502, FGFR2

N. diseases: 9
Disease: Apert syndrome ×
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.
Apert syndrome
CUI: C0001193
Disease: Apert syndrome
24 0.790 0.160 10 121517351 missense variant G/C snv 0.710 1.000 5 1996 2014