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: rs587777895
rs587777895
1 1.000 0.080 1 11139308 missense variant C/T snv 8.2E-06 2.1E-05 0.700 1.000 4 2015 2016