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: rs137854875
rs137854875
TSC2
1 1.000 0.120 16 2056769 missense variant G/C snv 0.700 1.000 16 1996 2005