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: rs120074176
rs120074176
TPH2
1 1.000 12 71979053 missense variant C/T snv 2.4E-05 0.800 1.000 1 2008 2008