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: rs4402960
rs4402960
21 0.724 0.400 3 185793899 intron variant G/T snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs6769511
rs6769511
2 0.925 0.120 3 185812502 intron variant T/C snv 0.46 0.700 1.000 1 2011 2011