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: rs3831732
rs3831732
2 10 87895485 intron variant -/A;AA delins 0.700 1.000 1 2016 2016
dbSNP: rs741804
rs741804
1 10 87896399 intron variant A/C snv 3.6E-02 0.700 1.000 1 2018 2018