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: rs10157197
rs10157197
1 1 150278225 intron variant G/A snv 0.40 0.700 1.000 2 2016 2016
dbSNP: rs10788873
rs10788873
1 1 150278123 intron variant T/A;C snv 0.60 0.700 1.000 1 2017 2017