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: rs204989
rs204989
2 0.925 0.120 6 32194075 intron variant G/A snv 0.21 0.020 1.000 2 2016 2016
dbSNP: rs204991
rs204991
3 0.882 0.200 6 32193589 intron variant T/C snv 0.21 0.010 1.000 1 2016 2016