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: rs10930831
rs10930831
1 2 178439249 non coding transcript exon variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs145766673
rs145766673
1 2 178424523 intron variant CTTT/- delins 0.19 0.700 1.000 1 2018 2018