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: rs79480822
rs79480822
1 1.000 0.080 17 63576864 intron variant C/T snv 3.8E-02 0.700 1.000 1 2016 2016