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: rs9590225
rs9590225
1 1.000 0.080 13 95263947 intron variant C/T snv 1.9E-02 0.700 1.000 1 2013 2013