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: rs1976714
rs1976714
1 3 123145924 intron variant G/T snv 0.32 0.700 1.000 2 2016 2017
dbSNP: rs16834024
rs16834024
1 3 123153306 intron variant G/A snv 5.2E-02 0.700 1.000 1 2017 2017