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: rs263232
rs263232
1 1.000 0.040 8 130795923 intron variant C/A snv 6.7E-02 0.800 1.000 1 2014 2014