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: rs869025292
rs869025292
1 1.000 0.080 9 136412502 missense variant C/T snv 0.800 1.000 2 2015 2016