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: rs17619601
rs17619601
1 1.000 0.080 13 28326373 intron variant C/T snv 5.0E-02 0.010 1.000 1 2012 2012