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: rs12000
rs12000
2 0.925 0.160 6 28259658 missense variant A/G snv 0.28 0.34 0.700 1.000 1 2009 2009
dbSNP: rs2235359
rs2235359
2 0.925 0.160 6 28247863 intron variant T/G snv 0.20 0.700 1.000 1 2009 2009