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: rs17012334
rs17012334
2 4 87059596 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs443459
rs443459
1 4 87054903 intron variant G/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs6819155
rs6819155
1 4 87055026 intron variant G/A snv 0.21 0.700 1.000 1 2018 2018