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: rs869320711
rs869320711
1 1.000 4 106233045 missense variant C/T snv 4.0E-06 0.800 1.000 3 2015 2016