Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs104893886
rs104893886
FGF10
1 1.000 0.280 5 44305155 missense variant A/C snv 0.800 1.000 2 2006 2006