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: rs6906662
rs6906662
6 0.882 0.200 6 32298729 intron variant G/A snv 6.8E-02 0.700 1.000 2 2009 2010
dbSNP: rs28732193
rs28732193
4 1.000 6 32339145 intron variant T/C snv 3.8E-02 0.700 1.000 1 2010 2010
dbSNP: rs28895018
rs28895018
4 1.000 6 32256601 intron variant T/C snv 6.8E-02 0.700 1.000 1 2010 2010
dbSNP: rs9391858
rs9391858
6 0.925 0.080 6 32373621 intron variant A/G snv 0.13 0.700 1.000 1 2010 2010