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: rs121918379
rs121918379
RDX
1 1.000 0.120 11 110231889 missense variant C/T snv 4.0E-06 0.800 1.000 1 2007 2007
dbSNP: rs121918380
rs121918380
RDX
1 1.000 0.120 11 110263964 stop gained G/A snv 0.700 0