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: rs121917782
rs121917782
1 16 67436264 missense variant C/T snv 4.0E-06 0.700 0
dbSNP: rs794726669
rs794726669
1 16 67435702 inframe deletion GAGTTG/- delins 7.0E-06 0.700 0