rs1554834892, FGF8

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.
Holoprosencephaly
CUI: C0079541
Disease: Holoprosencephaly
45 1.000 0.120 10 101774913 splice acceptor variant C/T snv 0.700 0