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: rs12949918
rs12949918
1 1.000 0.080 17 42374255 intron variant T/C snv 0.39 0.010 1.000 1 2011 2011
dbSNP: rs3816769
rs3816769
4 0.851 0.240 17 42346255 intron variant T/A;C snv 0.010 1.000 1 2013 2013
dbSNP: rs3869550
rs3869550
1 1.000 0.080 17 42340869 intron variant T/C snv 0.48 0.010 1.000 1 2011 2011
dbSNP: rs4796793
rs4796793
16 0.716 0.320 17 42390192 upstream gene variant G/C snv 0.67 0.010 1.000 1 2011 2011
dbSNP: rs7211777
rs7211777
3 0.882 0.120 17 42382057 intron variant G/A snv 0.52 0.010 1.000 1 2011 2011
dbSNP: rs744166
rs744166
22 0.689 0.560 17 42362183 intron variant A/G snv 0.48 0.010 1.000 1 2011 2011
dbSNP: rs9912773
rs9912773
1 1.000 0.080 17 42358516 intron variant C/A;G snv 0.010 1.000 1 2011 2011