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: rs2242446
rs2242446
9 0.776 0.080 16 55656513 5 prime UTR variant C/A;T snv 0.010 1.000 1 2008 2008
dbSNP: rs5558
rs5558
3 0.925 0.080 16 55699647 missense variant T/G snv 0.010 1.000 1 2009 2009
dbSNP: rs5569
rs5569
19 0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs7194256
rs7194256
7 0.827 0.120 16 55703779 3 prime UTR variant C/G;T snv 0.010 1.000 1 2017 2017