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: rs111906841
rs111906841
1 3 141242812 intron variant A/G snv 1.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs1346408
rs1346408
2 3 141353447 intron variant C/T snv 0.55 0.700 1.000 1 2019 2019
dbSNP: rs28721484
rs28721484
2 3 141334437 intron variant C/T snv 0.22 0.700 1.000 1 2017 2017
dbSNP: rs55768579
rs55768579
1 3 141340945 intron variant GA/- delins 1.3E-03 0.700 1.000 1 2017 2017