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: rs104893765
rs104893765
1 1.000 0.120 3 87262160 missense variant C/T snv 4.0E-06 0.800 1.000 12 1992 2016