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: rs2208532
rs2208532
3 0.882 0.080 2 31563919 intron variant G/A snv 0.59 0.010 1.000 1 2015 2015
dbSNP: rs523349
rs523349
21 0.689 0.440 2 31580636 missense variant G/A;C;T snv 0.66; 4.9E-06 0.010 1.000 1 2015 2015
dbSNP: rs676033
rs676033
3 0.882 0.080 2 31583901 upstream gene variant T/C snv 0.69 0.010 1.000 1 2015 2015