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: rs34211119
rs34211119
1 2 60493184 intron variant T/- delins 0.64 0.700 1.000 1 2016 2016
dbSNP: rs766432
rs766432
6 0.925 0.080 2 60492835 intron variant C/A snv 0.80 0.700 1.000 1 2016 2016