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: rs11576658
rs11576658
2 0.925 0.120 1 10977679 intron variant C/T snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs2003046
rs2003046
2 0.925 0.120 1 10972770 intron variant C/A;G snv 0.700 1.000 1 2012 2012