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: rs121434261
rs121434261
NF2
1 1.000 0.160 22 29636821 missense variant T/C snv 0.810 1.000 18 1993 2017