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: rs870288
rs870288
1 16 5535851 intron variant A/G snv 0.30 0.800 1.000 1 2012 2012
dbSNP: rs9924951
rs9924951
2 16 7454852 intron variant G/A snv 0.39 0.700 1.000 1 2008 2008