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: rs155979
rs155979
2 0.925 0.080 5 96434194 intron variant G/A;C snv 0.010 1.000 1 2014 2014
dbSNP: rs3762986
rs3762986
2 0.925 0.080 5 96435158 intron variant C/A;T snv 0.010 1.000 1 2014 2014