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: rs1154155
rs1154155
2 0.925 0.080 14 22533736 upstream gene variant G/A;T snv 0.010 1.000 1 2010 2010
dbSNP: rs12425451
rs12425451
3 0.882 0.080 12 3055757 TF binding site variant C/T snv 0.54 0.700 1.000 1 2013 2013
dbSNP: rs17212223
rs17212223
2 0.925 0.080 6 32683763 intergenic variant C/T snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs2859998
rs2859998
4 0.882 0.080 8 58411603 intron variant G/A snv 0.30 0.700 1.000 1 2013 2013
dbSNP: rs5770917
rs5770917
2 0.925 0.080 22 50578924 intron variant T/C snv 6.0E-02 0.010 1.000 1 2009 2009
dbSNP: rs9274477
rs9274477
2 0.925 0.080 6 32665936 intron variant A/G snv 0.700 1.000 1 2013 2013
dbSNP: rs7744020
rs7744020
3 0.882 0.160 6 32658353 upstream gene variant G/A snv 0.34 0.700 1.000 1 2013 2013