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: rs139459337
rs139459337
3 0.882 0.040 3 114997018 intron variant C/T snv 4.7E-02 0.700 1.000 1 2018 2018