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: rs150954431
rs150954431
2 1.000 0.080 12 124517777 intron variant C/T snv 1.6E-02 0.800 1.000 1 2014 2014