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: rs104894365
rs104894365
9 0.827 0.320 12 25245345 missense variant C/T snv 0.010 1.000 1 2016 2016