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: rs2619538
rs2619538
4 0.882 0.040 6 15664978 upstream gene variant A/T snv 0.54 0.050 0.800 5 2005 2010
dbSNP: rs9370822
rs9370822
7 0.882 0.120 6 15544505 intron variant A/C snv 0.36 0.030 1.000 3 2010 2011
dbSNP: rs1011313
rs1011313
1 1.000 0.040 6 15633201 intron variant T/A;C snv 0.020 1.000 2 2010 2014
dbSNP: rs1018381
rs1018381
6 0.882 0.040 6 15656839 intron variant G/A snv 0.16 0.020 1.000 2 2009 2009
dbSNP: rs2619539
rs2619539
3 0.925 0.040 6 15620624 intron variant C/A;G snv 0.020 1.000 2 2008 2009
dbSNP: rs16876759
rs16876759
1 1.000 0.040 6 15652070 intron variant T/C snv 4.8E-05 2.1E-05 0.010 1.000 1 2008 2008
dbSNP: rs1997679
rs1997679
6 0.882 0.120 6 15658674 intron variant G/A snv 0.35 0.010 1.000 1 2011 2011
dbSNP: rs2619522
rs2619522
6 0.827 0.080 6 15653418 intron variant A/C snv 0.26 0.010 1.000 1 2008 2008
dbSNP: rs2619528
rs2619528
2 1.000 0.040 6 15649598 intron variant C/T snv 0.26 0.010 1.000 1 2010 2010
dbSNP: rs3213207
rs3213207
11 0.776 0.120 6 15627871 intron variant T/C snv 8.7E-02 0.010 1.000 1 2008 2008
dbSNP: rs760666
rs760666
1 1.000 0.040 6 15588890 intron variant A/G snv 0.82 0.010 1.000 1 2007 2007
dbSNP: rs7758659
rs7758659
1 1.000 0.040 6 15593009 intron variant T/A;C snv 5.2E-06; 0.82 0.010 1.000 1 2007 2007
dbSNP: rs909706
rs909706
1 1.000 0.040 6 15660640 intron variant T/C snv 0.67 0.010 1.000 1 2009 2009