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: rs3861289
rs3861289
1 1.000 0.080 18 43111710 intron variant C/T snv 9.6E-02 0.700 1.000 1 2019 2019