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: rs507139
rs507139
2 1.000 11 225196 intron variant G/A snv 5.8E-02 0.700 1.000 1 2018 2018
dbSNP: rs547025
rs547025
2 1.000 11 232855 intron variant T/C snv 5.8E-02 0.700 1.000 1 2019 2019