rs1554552774, FGFR1

N. diseases: 2
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.
Kallmann Syndrome 2 (disorder)
CUI: C1563720
Disease: Kallmann Syndrome 2 (disorder)
45 0.925 0.200 8 38418227 splice donor variant C/T snv 0.700 1.000 1 2003 2003
Pfeiffer Syndrome
CUI: C0220658
Disease: Pfeiffer Syndrome
36 0.925 0.200 8 38418227 splice donor variant C/T snv 0.700 1.000 1 2003 2003