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: rs34233420
rs34233420
1 17 39848677 intron variant ATTT/- delins 0.700 1.000 1 2016 2016
dbSNP: rs9303277
rs9303277
9 0.790 0.240 17 39820216 intron variant C/T snv 0.52 0.700 1.000 1 2018 2018