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: rs398123045
rs398123045
TUBG1
1 1.000 17 42614845 missense variant T/C snv 0.800 0
dbSNP: rs398123046
rs398123046
TUBG1 ; RETREG3
1 1.000 17 42610535 splice donor variant A/G snv 0.800 0
dbSNP: rs398123047
rs398123047
TUBG1
1 1.000 17 42614407 missense variant A/C snv 0.800 0