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: rs2237897
rs2237897
6 0.882 0.200 11 2837316 intron variant C/T snv 8.1E-02 0.880 1.000 11 2008 2019