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: rs12527089
rs12527089
1 1.000 0.040 6 148466023 intron variant C/T snv 4.5E-02 0.700 1.000 1 2016 2016