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: rs17131023
rs17131023
1 1.000 0.080 1 69753508 intron variant T/C snv 3.5E-02 0.700 1.000 1 2009 2009