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: rs12365482
rs12365482
1 11 16591389 intron variant A/T snv 0.25 0.700 1.000 1 2016 2016
dbSNP: rs376898975
rs376898975
1 11 16737518 intron variant A/-;AA;AAA;AAAAA delins 0.700 1.000 1 2016 2016
dbSNP: rs72871339
rs72871339
1 11 16388953 intron variant C/T snv 1.8E-02 0.700 1.000 1 2016 2016