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: rs121913279
rs121913279
101 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs2677764
rs2677764
2 0.925 0.080 3 179206019 intron variant C/A;T snv 0.010 1.000 1 2011 2011
dbSNP: rs2699887
rs2699887
11 0.763 0.280 3 179148620 intron variant C/T snv 0.18 0.010 1.000 1 2012 2012
dbSNP: rs397517202
rs397517202
4 0.851 0.320 3 179234230 missense variant A/G snv 0.010 1.000 1 2007 2007
dbSNP: rs6443624
rs6443624
8 0.776 0.200 3 179179886 intron variant C/A snv 0.30 0.010 1.000 1 2012 2012
dbSNP: rs9838411
rs9838411
2 0.925 0.080 3 179169899 intron variant G/A snv 0.25 0.010 1.000 1 2012 2012