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: rs117758012
rs117758012
3 1.000 0.080 19 12846836 intron variant C/T snv 4.1E-02 0.700 1.000 1 2016 2016