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: rs3088362
rs3088362
1 1.000 0.040 13 43859494 intron variant C/A;T snv 0.710 1.000 3 2009 2016
dbSNP: rs9533634
rs9533634
1 1.000 0.040 13 43823679 downstream gene variant T/C snv 0.53 0.710 1.000 2 2009 2016