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: rs3809857
rs3809857
1 1.000 17 46770948 intron variant G/T snv 0.25 0.010 1.000 1 2018 2018
dbSNP: rs9890413
rs9890413
1 1.000 17 46824083 intron variant G/A snv 0.63 0.010 1.000 1 2018 2018