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: rs3134899
rs3134899
4 1.000 6 31505509 intron variant C/T snv 0.80 0.700 1.000 2 2009 2010
dbSNP: rs3828917
rs3828917
4 1.000 6 31498140 5 prime UTR variant G/A;T snv 0.700 1.000 2 2009 2010
dbSNP: rs2534657
rs2534657
6 0.882 0.200 6 31504682 intron variant C/T snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs2534678
rs2534678
5 0.925 0.120 6 31496186 intron variant G/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs3095234
rs3095234
4 1.000 6 31496794 intron variant C/A;T snv 0.700 1.000 1 2010 2010