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: rs9829778
rs9829778
2 3 196822218 intron variant G/A snv 0.53 0.700 1.000 2 2016 2019
dbSNP: rs7630852
rs7630852
1 3 196781680 intron variant T/A snv 0.53 0.700 1.000 1 2016 2016