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: rs7118648
rs7118648
1 1.000 0.040 11 96375264 intron variant T/C;G snv 7.5E-02 0.800 1.000 1 2013 2013