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: rs532553681
rs532553681
2 9 134037708 intron variant T/-;TT delins 0.700 1.000 1 2016 2016
dbSNP: rs72766630
rs72766630
3 9 134061669 intron variant G/A;T snv 0.700 1.000 1 2019 2019