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: rs75685923
rs75685923
1 1.000 0.080 9 133410109 intron variant C/T snv 2.0E-02 0.700 1.000 1 2017 2017