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: rs342702
rs342702
1 13 91770692 intron variant G/T snv 0.37 0.700 1.000 2 2018 2018
dbSNP: rs138994828
rs138994828
1 13 92028205 intron variant G/A snv 5.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs1929922
rs1929922
1 13 91799629 intron variant G/A snv 0.37 0.700 1.000 1 2019 2019