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: rs3830675
rs3830675
3 1.000 0.040 10 87931195 intron variant -/TCTTA delins 0.010 1.000 1 2019 2019