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: rs1011970
rs1011970
22 0.677 0.320 9 22062135 intron variant G/T snv 0.23 0.700 1.000 1 2016 2016
dbSNP: rs1412834
rs1412834
11 0.790 0.080 9 22110132 intron variant T/C snv 0.64 0.700 1.000 1 2019 2019
dbSNP: rs1537372
rs1537372
14 0.752 0.120 9 22103184 intron variant G/A;T snv 0.700 1.000 1 2019 2019