rs199573818, FGFR1

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.
Kallmann Syndrome
CUI: C0162809
Disease: Kallmann Syndrome
30 1.000 0.160 8 38417882 missense variant T/C;G snv 0.010 1.000 1 2014 2014