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: rs3740390
rs3740390
1 0.925 0.080 10 102878723 intron variant C/T snv 9.2E-02 0.700 1.000 1 2018 2018