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: rs1970000
rs1970000
1 1.000 0.200 9 5465036 intron variant C/A;G snv 0.010 1.000 1 2011 2011