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: rs2160322
rs2160322
5 0.851 0.160 7 78462650 intron variant G/A;C snv 0.010 1.000 1 2009 2009
dbSNP: rs6962966
rs6962966
3 0.925 0.120 7 78174806 intron variant A/G snv 0.50 0.010 1.000 1 2017 2017