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: rs158676
rs158676
2 0.925 0.040 20 33386589 intron variant G/A snv 0.68 0.010 1.000 1 2013 2013
dbSNP: rs291700
rs291700
3 0.925 0.040 20 33394043 synonymous variant T/C snv 0.64 0.62 0.010 1.000 1 2013 2013