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: rs1557211209
rs1557211209
LAGE3 ; PLXNA3
1 1.000 X 154477966 missense variant A/G snv 0.800 0
dbSNP: rs1557211306
rs1557211306
LAGE3
1 1.000 X 154478284 missense variant C/A snv 0.800 0
dbSNP: rs1557211410
rs1557211410
LAGE3
1 1.000 X 154478727 splice donor variant C/T snv 0.700 0