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: rs143072280
rs143072280
1 1.000 0.080 10 38105003 intron variant -/CTTT delins 0.40 0.700 1.000 1 2017 2017