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: rs1671021
rs1671021
LLGL2
2 1.000 0.080 17 75569090 missense variant T/C snv 0.36 0.50 0.020 1.000 2 2009 2011