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: rs10852622
rs10852622
2 16 88490472 intron variant A/G snv 0.35 0.700 1.000 1 2016 2016
dbSNP: rs118090537
rs118090537
1 16 88493354 intron variant G/A snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs17175830
rs17175830
1 16 88491756 intron variant G/A;C;T snv 0.700 1.000 1 2019 2019