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: rs3024493
rs3024493
9 0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs1878672
rs1878672
3 0.882 0.080 1 206770368 intron variant G/A;C;T snv 0.010 1.000 1 2015 2015
dbSNP: rs3024490
rs3024490
11 0.742 0.520 1 206771966 intron variant A/C;G;T snv 0.010 1.000 1 2015 2015