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: rs58461606
rs58461606
1 2 267367 intron variant G/T snv 0.30 0.700 1.000 1 2018 2018
dbSNP: rs79716074
rs79716074
1 2 277003 missense variant A/G snv 0.31 0.30 0.700 1.000 1 2018 2018