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: rs1060505035
rs1060505035
1 1.000 5 82276183 missense variant A/T snv 0.800 1.000 1 2017 2017
dbSNP: rs1060505034
rs1060505034
1 1.000 5 82276483 missense variant C/T snv 0.800 1.000 1 2017 2017