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: rs7281353
rs7281353
1 1.000 0.080 21 21779123 intron variant C/G snv 0.76 0.700 1.000 1 2017 2017