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: rs12425451
rs12425451
2 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
2 0.882 0.080 8 58411603 intron variant G/A snv 0.30 0.700 1.000 1 2013 2013
dbSNP: rs7744020
rs7744020
2 0.882 0.160 6 32658353 upstream gene variant G/A snv 0.34 0.700 1.000 1 2013 2013
dbSNP: rs9274477
rs9274477
2 0.925 0.080 6 32665936 intron variant A/G snv 0.700 1.000 1 2013 2013