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: rs2069639
rs2069639
1 5 132075408 intron variant A/T snv 1.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs25884
rs25884
2 5 132076545 upstream gene variant A/G snv 0.31 0.700 1.000 1 2016 2016