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: rs1799990
rs1799990
2 0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 0.900 1.000 1 1996 2015
dbSNP: rs6107516
rs6107516
2 1.000 0.120 20 4696446 intron variant G/A snv 0.23 0.800 1.000 1 2012 2012