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: rs13220495
rs13220495
3 0.925 0.160 6 26441412 intron variant C/T snv 5.3E-02 0.700 1.000 1 2019 2019