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: rs34135146
rs34135146
1 1.000 0.040 3 52279416 intron variant G/C snv 9.3E-02 0.700 1.000 1 2018 2018