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: rs750496798
rs750496798
1 1.000 0.120 4 1002383 missense variant C/T snv 8.3E-06 0.700 1.000 8 1993 2011