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: rs775266057
rs775266057
1 1.000 0.080 8 116847532 missense variant C/T snv 8.0E-06 0.800 1.000 1 2015 2015